Mansoor Khan
#168,095
Most Influential Person Now
Researcher ORCID 0000-0003-3649-3874
Mansoor Khan's AcademicInfluence.com Rankings
Mansoor Khancomputer-science Degrees
Computer Science
#10244
World Rank
#10740
Historical Rank
Computational Linguistics
#2588
World Rank
#2613
Historical Rank
Machine Learning
#4687
World Rank
#4739
Historical Rank
Artificial Intelligence
#5050
World Rank
#5115
Historical Rank
Download Badge
Computer Science
Mansoor Khan's Degrees
- PhD Computer Science Stanford University
- Masters Computer Science University of California, Berkeley
- Bachelors Computer Engineering University of California, Berkeley
Similar Degrees You Can Earn
Why Is Mansoor Khan Influential?
(Suggest an Edit or Addition)Mansoor Khan's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Understanding Pharmaceutical Quality by Design (2014) (746)
- A new chapter in pharmaceutical manufacturing: 3D‐printed drug products☆, ☆☆ (2017) (536)
- Targeting to macrophages: role of physicochemical properties of particulate carriers--liposomes and microspheres--on the phagocytosis by macrophages. (2002) (517)
- Comparative Evaluation of Flow for Pharmaceutical Powders and Granules (2008) (341)
- Assessment of Recent Process Analytical Technology (PAT) Trends: A Multiauthor Review (2015) (297)
- Preparation and in vitro characterization of a eutectic based semisolid self-nanoemulsified drug delivery system (SNEDDS) of ubiquinone: mechanism and progress of emulsion formation. (2002) (256)
- Absorption enhancers in pulmonary protein delivery. (2004) (164)
- Non-destructive methods of characterization of risperidone solid lipid nanoparticles. (2010) (156)
- Understanding the quality of protein loaded PLGA nanoparticles variability by Plackett-Burman design. (2010) (146)
- Controlled release of a self-emulsifying formulation from a tablet dosage form: stability assessment and optimization of some processing parameters. (2006) (144)
- Quality by design: understanding the formulation variables of a cyclosporine A self-nanoemulsified drug delivery systems by Box-Behnken design and desirability function. (2007) (143)
- A quality by design (QbD) case study on liposomes containing hydrophilic API: I. Formulation, processing design and risk assessment. (2011) (129)
- Preparation and in vitro characterization of self-nanoemulsified drug delivery system (SNEDDS) of all-trans-retinol acetate. (2004) (122)
- Preparation and characterization of magnetic allylamine modified graphene oxide-poly(vinyl acetate-co-divinylbenzene) nanocomposite for vortex assisted magnetic solid phase extraction of some metal ions. (2016) (115)
- Physico-mechanical and Stability Evaluation of Carbamazepine Cocrystal with Nicotinamide (2011) (113)
- Application of quality by design elements for the development and optimization of an analytical method for protamine sulfate. (2012) (109)
- Quantitative determination of cesium binding to ferric hexacyanoferrate: Prussian blue. (2008) (107)
- Oral delivery of proteins: progress and prognostication. (2002) (106)
- A quality by design (QbD) case study on liposomes containing hydrophilic API: II. Screening of critical variables, and establishment of design space at laboratory scale. (2012) (99)
- Predicting hydrophilic drug encapsulation inside unilamellar liposomes. (2012) (98)
- Quality-by-design (QbD): an integrated multivariate approach for the component quantification in powder blends. (2009) (96)
- Quality-by-Design (QbD): An integrated process analytical technology (PAT) approach for a dynamic pharmaceutical co-precipitation process characterization and process design space development. (2011) (95)
- A Report from the Pediatric Formulations Task Force: Perspectives on the State of Child-Friendly Oral Dosage Forms (2013) (93)
- Response surface methodology for the optimization of ubiquinone self-nanoemulsified drug delivery system (2008) (92)
- Optimization and characterization of controlled release pellets coated with an experimental latex: II. Cationic drug (1995) (87)
- Crystallinity evaluation of tacrolimus solid dispersions by chemometric analysis. (2012) (86)
- A two-stage reverse dialysis in vitro dissolution testing method for passive targeted liposomes. (2012) (80)
- Risperidone solid dispersion for orally disintegrating tablet: its formulation design and non-destructive methods of evaluation. (2010) (80)
- Tablet Splitting of a Narrow Therapeutic Index Drug: A Case with Levothyroxine Sodium (2010) (77)
- Building better drugs: developing and regulating engineered therapeutic proteins. (2013) (76)
- Real-time on-line blend uniformity monitoring using near-infrared reflectance spectrometry: a noninvasive off-line calibration approach. (2009) (76)
- Process analytical technology: chemometric analysis of Raman and near infra-red spectroscopic data for predicting physical properties of extended release matrix tablets. (2007) (74)
- Quality by design: impact of formulation variables and their interactions on quality attributes of a lyophilized monoclonal antibody. (2012) (74)
- Box-behnken design for the optimization of formulation variables of indomethacin coprecipitates with polymer mixtures (1996) (72)
- Development and evaluation of paclitaxel nanoparticles using a quality-by-design approach. (2013) (71)
- Atenolol gastrointestinal therapeutic system: optimization of formulation variables using response surface methodology (1997) (69)
- Current Status of the Oral Delivery of Insulin (2001) (68)
- Preparation and Characterization of Coenzyme Q10–Eudragit® Solid Dispersion (2002) (68)
- Development of performance matrix for generic product equivalence of acyclovir topical creams. (2014) (66)
- Evaluation of cytotoxicity of oils used in coenzyme Q10 Self-emulsifying Drug Delivery Systems (SEDDS). (2004) (65)
- Quality-by-design (QbD): an integrated approach for evaluation of powder blending process kinetics and determination of powder blending end-point. (2009) (64)
- Process analytical technology (PAT): quantification approaches in terahertz spectroscopy for pharmaceutical application. (2008) (63)
- Process analytical technology (PAT): effects of instrumental and compositional variables on terahertz spectral data quality to characterize pharmaceutical materials and tablets. (2007) (62)
- Impact of controlled ice nucleation on process performance and quality attributes of a lyophilized monoclonal antibody. (2013) (62)
- Application of quality by design to formulation and processing of protein liposomes. (2012) (62)
- Defining Patient Centric Pharmaceutical Drug Product Design (2016) (61)
- Additive Manufacturing with 3D Printing: Progress from Bench to Bedside (2018) (60)
- Development and validation of in vitro-in vivo correlation (IVIVC) for estradiol transdermal drug delivery systems. (2015) (59)
- Selective laser sintering 3D printing – an overview of the technology and pharmaceutical applications (2020) (58)
- Participation of women in clinical trials for new drugs approved by the food and drug administration in 2000-2002. (2009) (57)
- A small variation in average particle size of PLGA nanoparticles prepared by nanoprecipitation leads to considerable change in nanoparticles’ characteristics and efficacy of intracellular delivery (2017) (57)
- Optimization and characterization of controlled release multi-particulate beads coated with starch acetate. (2005) (56)
- PROCESS CONTROL PERSPECTIVE FOR PROCESS ANALYTICAL TECHNOLOGY: INTEGRATION OF CHEMICAL ENGINEERING PRACTICE INTO SEMICONDUCTOR AND PHARMACEUTICAL INDUSTRIES (2007) (55)
- Quality-by-design (QbD): effects of testing parameters and formulation variables on the segregation tendency of pharmaceutical powder measured by the ASTM D 6940-04 segregation tester. (2008) (54)
- Optimization and characterization of controlled release multi-particulate beads formulated with a customized cellulose acetate butyrate dispersion. (2002) (54)
- Understanding the effects of formulation and process variables on the printlets quality manufactured by selective laser sintering 3D printing. (2019) (54)
- Development and application of a validated HPLC method for the determination of gabapentin and its major degradation impurity in drug products. (2007) (52)
- Formulation and process factors influencing product quality and in vitro performance of ophthalmic ointments. (2015) (52)
- Vortex assisted magnetic solid phase extraction of lead(II) and cobalt(II) on silica coated magnetic multiwalled carbon nanotubes impregnated with 1-(2-pyridylazo)-2-naphthol (2016) (51)
- Disintegration of Highly Soluble Immediate Release Tablets: A Surrogate for Dissolution (2009) (50)
- Near-Infrared Investigations of Novel Anti-HIV Tenofovir Liposomes (2010) (48)
- Response surface methodology for optimization and characterization of limonene-based coenzyme Q10 self-nanoemulsified capsule dosage form (2004) (48)
- A quantitative study of the effect of process parameters on key granule characteristics in a high shear wet granulation process involving a two component pharmaceutical blend (2015) (47)
- A mechanistic population balance model for granulation processes: Effect of process and formulation parameters (2014) (45)
- Quality by design in formulation and process development for a freeze-dried, small molecule parenteral product: a case study (2011) (44)
- Robust calibration design in the pharmaceutical quantitative measurements with near-infrared (NIR) spectroscopy: Avoiding the chemometric pitfalls. (2009) (44)
- Influence of Formulation and Processing Factors on Stability of Levothyroxine Sodium Pentahydrate (2010) (44)
- Quality-by-Design (QbD): an integrated process analytical technology (PAT) approach for real-time monitoring and mapping the state of a pharmaceutical coprecipitation process. (2010) (42)
- Product and process understanding of a novel pediatric anti-HIV tenofovir niosomes with a high-pressure homogenizer. (2011) (41)
- Switchable solvent based liquid phase microextraction of mercury from environmental samples: a green aspect (2016) (41)
- Preparation and characterization of genistein containing poly(ethylene glycol) microparticles (2006) (40)
- Strategies of targeting oral drug delivery systems to the colon and their potential use for the treatment of colorectal cancer (2012) (40)
- Quantitative determination of thallium binding to ferric hexacyanoferrate: Prussian blue. (2008) (39)
- Synthesis and Evaluation of Morpholinoalkyl Ester Prodrugs of Indomethacin and Naproxen (1993) (39)
- Improvement of Physicochemical Properties of an Antiepileptic Drug by Salt Engineering (2012) (39)
- Switchable solvent based liquid phase microextraction of uranium in environmental samples: a green approach (2016) (38)
- Considerations for a Pediatric Biopharmaceutics Classification System (BCS): Application to Five Drugs (2014) (37)
- Quality by design approach for understanding the critical quality attributes of cyclosporine ophthalmic emulsion. (2014) (37)
- Permeability of Chemical Delivery Systems Across Rabbit Corneal (SIRC) Cell Line and Isolated Corneas: A Comparative Study (2000) (36)
- Assessing impact of formulation and process variables on in-vitro performance of directly compressed abuse deterrent formulations. (2016) (36)
- Transport studies of insulin across rat jejunum in the presence of chicken and duck ovomucoids (2001) (36)
- Bioavailability Assessment of Oral Coenzyme Q10 Formulations in Dogs (2002) (36)
- Development and optimization of taste-masked orally disintegrating tablets (ODTs) of clindamycin hydrochloride (2015) (35)
- Fabrication of stable superabsorbent hydrogels for successful removal of crystal violet from waste water (2019) (34)
- Tablet splitting: Product quality assessment of metoprolol succinate extended release tablets. (2010) (34)
- Development and validation of an ion chromatography method for the determination of phosphate-binding of lanthanum carbonate. (2010) (34)
- Atenolol Gastrointestinal Therapeutic System. I. Screening of Formulation Variables (1997) (33)
- Optimization of process variables for the preparation of ibuprofen coprecipitates with Eudragit S100 (1994) (33)
- THz spectroscopy: An emerging technology for pharmaceutical development and pharmaceutical Process Analytical Technology (PAT) applications (2012) (32)
- Orally disintegrating tablet of novel salt of antiepileptic drug: formulation strategy and evaluation. (2013) (32)
- Physicochemical and mechanical properties of carbamazepine cocrystals with saccharin (2012) (32)
- Controlled release coprecipitates : formulation considerations (1995) (32)
- Zwitterionic superabsorbent polymer hydrogels for efficient and selective removal of organic dyes (2019) (32)
- Formulation Optimization of Selective Laser Sintering 3D-Printed Tablets of Clindamycin Palmitate Hydrochloride by Response Surface Methodology (2020) (32)
- Kinetics of drug release from ointments: Role of transient-boundary layer. (2015) (31)
- Development and application of a validated HPLC method for the analysis of dissolution samples of gabapentin drug products. (2008) (31)
- Complexation of risperidone with a taste-masking resin: Novel application of near infra-red and chemical imaging to evaluate complexes (2009) (31)
- Drug product characterization by macropixel analysis of chemical images. (2007) (30)
- An Integrated Process Analytical Technology (PAT) Approach for Pharmaceutical Crystallization Process Understanding to Ensure Product Quality and Safety: FDA Scientist’s Perspective (2015) (30)
- Chain length-dependent effects of alkylmaltosides on nasal absorption of enoxaparin. (2004) (30)
- Formulation and Evaluation of a Protein-loaded Solid Dispersions by Non-destructive Methods (2010) (30)
- Pharmaceutical characterization of novel tenofovir liposomal formulations for enhanced oral drug delivery: in vitro pharmaceutics and Caco-2 permeability investigations (2017) (30)
- NIR Spectroscopy Applications in the Development of a Compacted Multiparticulate System for Modified Release (2011) (30)
- 3D-printing of lopinavir printlets by selective laser sintering and quantification of crystalline fraction by XRPD-chemometric models. (2020) (30)
- Quality by Design for Biopharmaceutical Drug Product Development (2015) (29)
- Online Monitoring of PLGA Microparticles Formation Using Lasentec Focused Beam Reflectance (FBRM) and Particle Video Microscope (PVM) (2010) (29)
- Quality by design: understanding the product variability of a self-nanoemulsified drug delivery system of cyclosporine A. (2007) (29)
- Response Surface Methodology for the Development of Self-Nanoemulsified Drug Delivery System (SNEDDS) of All-Trans-Retinol Acetate (2005) (29)
- Protection of salmon calcitonin breakdown with serine proteases by various ovomucoid species for oral drug delivery. (2004) (28)
- Fermentanomics: Relating quality attributes of a monoclonal antibody to cell culture process variables and raw materials using multivariate data analysis (2015) (28)
- Influence of drug loading and type of ointment base on the in vitro performance of acyclovir ophthalmic ointment. (2015) (28)
- Chemometric Model Development and Comparison of Raman and (13)C Solid-State Nuclear Magnetic Resonance-Chemometric Methods for Quantification of Crystalline/Amorphous Warfarin Sodium Fraction in the Formulations. (2015) (28)
- Oral Delivery of Proteins: Effect of Chicken and Duck Ovomucoid on the Stability of Insulin in the Presence of α‐Chymotrypsin and Trypsin (2000) (28)
- Cytotoxicity evaluation of enzyme inhibitors and absorption enhancers in Caco-2 cells for oral delivery of salmon calcitonin. (2004) (27)
- Regional permeability of salmon calcitonin in isolated rat gastrointestinal tracts: Transport mechanism using Caco-2 cell monolayer (2004) (26)
- Effect of Extragranular Microcrystalline Cellulose on Compaction, Surface Roughness, and In Vitro Dissolution of a Self-Nanoemulsified Solid Dosage Form of Ubiquinone (2002) (25)
- Assessing the impact of nimodipine devitrification in the ternary cosolvent system through quality by design approach. (2013) (25)
- Preparation and characterization of a customized cellulose acetate butyrate dispersion for controlled drug delivery. (2002) (25)
- Risk based in vitro performance assessment of extended release abuse deterrent formulations. (2016) (25)
- Chemometric methods for the quantification of crystalline tacrolimus in solid dispersion by powder X-ray diffractrometry. (2014) (25)
- Comparison of the stability of split and intact gabapentin tablets. (2008) (24)
- Effects of excipients and curing process on the abuse deterrent properties of directly compressed tablets. (2017) (24)
- Physicochemical Characterization of Complex Drug Substances: Evaluation of Structural Similarities and Differences of Protamine Sulfate from Various Sources (2012) (23)
- Tannate complexes of antihistaminic drug: sustained release and taste masking approaches. (2012) (23)
- Comparison of X-ray powder diffraction and solid-state nuclear magnetic resonance in estimating crystalline fraction of tacrolimus in sustained-release amorphous solid dispersion and development of discriminating dissolution method. (2015) (23)
- Comparison of raloxifene and bisphosphonates based on adherence and treatment satisfaction in postmenopausal Asian women (2007) (23)
- United States Food and Drug Administration and Department of Defense shelf-life extension program of pharmaceutical products: progress and promise. (2014) (22)
- Combination of Paclitaxel and R-flurbiprofen loaded PLGA nanoparticles suppresses glioblastoma growth on systemic administration. (2020) (21)
- Supramolecular solvent based liquid–liquid microextraction of aluminum from water and hair samples prior to UV-visible spectrophotometric detection (2015) (21)
- Formulation and transport properties of tenofovir loaded liposomes through Caco-2 cell model (2013) (20)
- Aqueous-based polymeric dispersion: preparation and characterization of cellulose acetate pseudolatex (1998) (20)
- Liposome Formation Using a Coaxial Turbulent Jet in Co-Flow (2016) (20)
- Oseltamivir phosphate-amberlite(TM) IRP 64 ionic complex for taste masking: preparation and chemometric evaluation. (2013) (20)
- Compression of Indomethacin Coprecipitates with Polymer Mixtures: Effect of Preparation Methodology (1995) (20)
- Statistical Optimization of Ketoprofen-Eudragit® S100 Coprecipitates to Obtain Controlled-Release Tablets (1996) (20)
- Thermodynamic stability assessment of a colloidal iron drug product: sodium ferric gluconate. (2010) (20)
- Chemometric evaluation of near infrared, fourier transform infrared, and Raman spectroscopic models for the prediction of nimodipine polymorphs. (2013) (20)
- Cholorpheniramine tannate complexes: physicochemical, chemometric, and taste masking evaluation. (2012) (19)
- Synthesis of physically cross-linked gum Arabic-based polymer hydrogels with enhanced mechanical, load bearing and shape memory behavior (2020) (19)
- Controlled Release Multiparticulate Beads Coated with Starch Acetate: Material Characterization, and Identification of Critical Formulation and Process Variables (2007) (19)
- Stability Characterization, Kinetics and Mechanism of Degradation of Dantrolene in Aqueous Solution: Effect of pH and Temperature (2012) (19)
- Quantitative estimation of phenytoin sodium disproportionation in the formulations using vibration spectroscopies and multivariate methodologies. (2018) (18)
- Use of In Vitro–In Vivo Correlation to Predict the Pharmacokinetics of Several Products Containing a BCS Class 1 Drug in Extended Release Matrices (2012) (18)
- Effect of Ethanol on Opioid Drug Permeability Through Caco-2 Cell Monolayers (2008) (18)
- Improved Stability of a Model IgG3 by DoE-Based Evaluation of Buffer Formulations (2016) (18)
- Removal and recovery of cadmium from aqueous solutions using magnetic nanoparticle-modified sawdust: kinetics and adsorption isotherm studies (2016) (18)
- Complexation between risperidone and amberlite resin by various methods of preparation and binding study (2009) (17)
- Process analytical technology: nondestructive evaluation of cyclosporine A and phospholipid solid dispersions by near infrared spectroscopy and imaging. (2008) (17)
- Near-infrared and fourier transform infrared chemometric methods for the quantification of crystalline tacrolimus from sustained-release amorphous solid dispersion. (2014) (17)
- Application of NIR chemometric methods for quantification of the crystalline fraction of warfarin sodium in drug product (2016) (17)
- Functionality of magnesium stearate derived from bovine and vegetable sources: dry granulated tablets. (2008) (17)
- Understanding effect of formulation and manufacturing variables on the critical quality attributes of warfarin sodium product. (2015) (17)
- Evaluation of Transmission and Reflection Modalities for Measuring Content Uniformity of Pharmaceutical Tablets with Near-Infrared Spectroscopy (2009) (17)
- An integrated process analytical technology (PAT) approach to monitoring the effect of supercooling on lyophilization product and process parameters of model monoclonal antibody formulations. (2014) (17)
- Spectroscopic-Based Chemometric Models for Quantifying Low Levels of Solid-State Transitions in Extended Release Theophylline Formulations. (2016) (16)
- Synthesis of graphene oxide doped poly(2-acrylamido-2-methyl propane sulfonic acid) [GO@p(AMPS)] composite hydrogel with pseudo-plastic thixotropic behavior (2019) (16)
- Biodegradable Microparticulates of Beta-Estradiol: Preparation and In Vitro Characterization (2005) (16)
- Product and process understanding to relate the effect of freezing method on glycation and aggregation of lyophilized monoclonal antibody formulations. (2015) (16)
- Influence of tablet characteristics on weight variability and weight loss in split tablets. (2008) (16)
- Chemometric Models for Quantification of Carbamazepine Anhydrous and Dihydrate Forms in the Formulation. (2019) (16)
- Adsorption and recovery of hexavalent chromium from tannery wastewater over magnetic max phase composite (2020) (16)
- Root cause evaluation of particulates in the lyophilized indomethacin sodium trihydrate plug for parenteral administration. (2014) (16)
- Advancing Product Quality: a Summary of the Inaugural FDA/PQRI Conference (2015) (16)
- Quality-by-design: an integrated process analytical technology approach to determine the nucleation and growth mechanisms during a dynamic pharmaceutical coprecipitation process. (2011) (16)
- In vitro bioequivalence approach for a locally acting gastrointestinal drug: lanthanum carbonate. (2013) (16)
- Development and validation of X-ray diffraction method for quantitative determination of crystallinity in warfarin sodium products. (2015) (15)
- Preparation and characterization of a suite of ephedra-containing standard reference materials. (2006) (15)
- Effect of processing parameters and controlled environment storage on the disproportionation and dissolution of extended‐release capsule of phenytoin sodium (2018) (15)
- Stability of gabapentin 300-mg capsules repackaged in unit dose containers. (2009) (15)
- Blend of cellulose ester and enteric polymers for delayed and enteric coating of core tablets of hydrophilic and hydrophobic drugs. (2019) (15)
- Evaluation of In-Use Stability of Anticoagulant Drug Products: Warfarin Sodium. (2015) (15)
- Integrated Process Analytical Technology Approach for Nucleation Induction Time Measurement and Nucleation Mechanism Assessment for a Dynamic Multicomponent Pharmaceutical Antisolvent Crystallization System (2014) (15)
- Quality by Design (2017) (15)
- Challenges of pediatric formulations: a FDA science perspective. (2013) (15)
- Spectral and spatial characterization of protein loaded PLGA nanoparticles. (2010) (14)
- Evaluation of Abuse-Deterrent Characteristics of Tablets Prepared via Hot-Melt Extrusion (2019) (14)
- An Integrated Process Analytical Technology (PAT) Approach for Process Dynamics-Related Measurement Error Evaluation and Process Design Space Development of a Pharmaceutical Powder Blending Bed (2015) (14)
- Salbutamol Sulfate Suppositories: Influence of Formulation on Physical Parameters and Stability (2003) (14)
- Real time monitoring of bioreactor mAb IgG3 cell culture process dynamics via Fourier transform infrared spectroscopy: Implications for enabling cell culture process analytical technology (2015) (14)
- Difference in the Lubrication Efficiency of Bovine and Vegetable-Derived Magnesium Stearate During Tabletting (2009) (14)
- Determination of tacrolimus crystalline fraction in the commercial immediate release amorphous solid dispersion products by a standardized X-ray powder diffraction method with chemometrics. (2014) (14)
- Solid phase extraction of uranium(VI) on phosphorus-containing polymer grafted 4-aminoantipyrine (2016) (14)
- Nanopharmaceuticals: Challenges and Regulatory Perspective (2009) (13)
- Dose Uniformity of Scored and Unscored Tablets: Application of the FDA Tablet Scoring Guidance for Industry (2016) (13)
- Characterization and selection of suitable grades of lactose as functional fillers for capsule filling: part 1 (2015) (13)
- Pharmaceutical characterization and thermodynamic stability assessment of a colloidal iron drug product: iron sucrose. (2014) (13)
- Impact of formulation and process variables on solid-state stability of theophylline in controlled release formulations. (2016) (13)
- Development and Validation of a HPLC Method for Dissolution and Stability Assay of Liquid-Filled Cyclosporine Capsule Drug Products (2013) (12)
- Percutaneous permeation of enantiomers and racemates of chiral drugs and prediction of their flux ratios using thermal data: a pharmaceutical perspective. (2003) (12)
- Effect of Additives on the Diffusion of Ketoprofen Through Human Skin (1996) (12)
- Supramolecular solvent microextraction of uranium at trace levels from water and soil samples (2017) (12)
- Comparative stability of repackaged metoprolol tartrate tablets. (2010) (12)
- A QbD Case Study: Bayesian Prediction of Lyophilization Cycle Parameters (2011) (12)
- Stability of ranitidine syrup re-packaged in unit-dose containers. (2008) (12)
- Development of a HPLC method for the determination of cyclosporin-A in rat blood and plasma using naproxen as an internal standard. (2003) (12)
- Printing of personalized medication using binder jetting 3D printer (2020) (12)
- Development of High Temperature High Pressure (HTHP) Water Based Drilling Mud using Synthetic Polymers, and Nanoparticles (2018) (11)
- Synthesis and Rheological Survey of Xanthan Gum Based Terpolymeric Hydrogels (2020) (11)
- An index for evaluating difficulty of Chewing Index for chewable tablets (2015) (11)
- Comparative evaluation of the in vitro efficacy of lanthanum carbonate chewable tablets. (2013) (11)
- Long-term stability study of Prussian blue - a quality assessment of water content and thallium binding. (2014) (11)
- Development and Validation of a Discriminatory Dissolution Method for Rifaximin Products. (2019) (10)
- Evaluation of butyrate‐induced production of a mannose‐6‐phosphorylated therapeutic enzyme using parallel bioreactors (2014) (10)
- Regulatory Considerations in Development of Amorphous Solid Dispersions (2014) (10)
- Hunter screening design to understand the product variability of solid dispersion formulation of a peptide antibiotic. (2013) (10)
- Hot‐Melt Extrusion: An FDA Perspective on Product and Process Understanding (2012) (10)
- Fractionated charge variants of biosimilars: A review of separation methods, structural and functional analysis. (2021) (10)
- Integration of Near-Infrared Spectroscopy and Mechanistic Modeling for Predicting Film-Coating and Dissolution of Modified Release Tablets (2015) (10)
- Ultra-long Acting Prodrug of Dolutegravir and Delivery System - Physicochemical, Pharmacokinetic and Formulation Characterizations. (2021) (10)
- Non-enzymatic colorimetric biosensor for hydrogen peroxide using lignin-based silver nanoparticles tuned with ionic liquid as a peroxidase mimic (2021) (10)
- Response Surface Methodology to Obtain β-Estradiol Biodegradable Microspheres for Long-Term Therapy of Osteoporosis (2006) (9)
- Controlled drug delivery. Development of solid oral dosage forms with acrylate polymers (1997) (9)
- Plackett-Burman screening of micromatrices with polymer mixtures for controlled drug delivery (1995) (9)
- Characterization of a nonribosomal peptide antibiotic solid dispersion formulation by process analytical technologies sensors. (2013) (9)
- Pharmaceutical and Clinical Calculations (2000) (9)
- Quality by Design (QbD), Biopharmaceutical Manufacture (2010) (8)
- A long-term stability study of Prussian blue: A quality assessment of water content and cesium binding. (2015) (8)
- Intraocular Pressure-Lowering Activity and In Vivo Disposition of Dipivalyl Terbutalone in Rabbits (2001) (8)
- Development of Abuse-Deterrent Formulations Using Sucrose Acetate Isobutyrate (2020) (8)
- Nanoparticles for improvement in oral bioavailability (2019) (8)
- Magnetic Solid Phase Extraction of Lead, Cadmium, and Cobalt on Magnetic Carboxyl-Modified Nanodiamonds (MCNDs) from Natural Water Samples and Their Determination by Flame Atomic Absorption Spectrometry (2018) (8)
- Development and Application of a Validated HPLC Method for the Determination of Clindamycin Palmitate Hydrochloride in Marketed Drug Products: An Optimization of the Current USP Methodology for Assay (2013) (7)
- Development Of Methamphetamine Abuse-Deterrent Formulations Using Sucrose Acetate Isobutyrate. (2019) (7)
- Very-Rapidly Dissolving Printlets of Isoniazid Manufactured by SLS 3D Printing: In Vitro and In Vivo Characterization. (2022) (7)
- Process analytical technology to understand the disintegration behavior of alendronate sodium tablets. (2013) (7)
- Focused beam reflectance measurement to monitor nimodipine precipitation process. (2013) (7)
- Ibuprofen Release from Beads Coated with an Experimental Latex: Effect of Certain Variables (1997) (7)
- Influence of psychostimulants and opioids on epigenetic modification of class III histone deacetylase (HDAC)-sirtuins in glial cells (2021) (7)
- Cold flow of estradiol transdermal systems: influence of drug loss on the in vitro flux and drug transfer across human epidermis. (2014) (7)
- Quality and In-Use Stability Comparison of Brand and Generics of Extended-Release Phenytoin Sodium Capsules. (2019) (7)
- Comparative evaluation of in vitro efficacy of colesevelam hydrochloride tablets (2014) (7)
- Development and application of a validated stability-indicating Ultra-Performance Liquid Chromatography (UPLC) method for the determination of dantrolene and its related impurities (2010) (7)
- Analytical methods for the evaluation of melamine contamination. (2014) (6)
- Evaluation of the In Vitro Efficacy of Sevelamer Hydrochloride and Sevelamer Carbonate. (2016) (6)
- Comparison of Univariate and Multivariate Models of 13C SSNMR and XRPD Techniques for Quantification of Nimodipine Polymorphs (2015) (6)
- Development of a Validated Stability Indicating HPLC Method for Ranitidine Hydrochloride Syrup (2006) (6)
- Aqueous-Based Cellulose Acetate Butyrate Dispersion: Screening of Process and Formulation Variables to Obtain Verapamil HCl-Controlled Release Beads (2001) (6)
- Stereomicroscopic imaging technique for the quantification of cold flow in drug-in-adhesive type of transdermal drug delivery systems. (2014) (6)
- Application of salt engineering to reduce/mask bitter taste of clindamycin (2019) (6)
- Implementation of a New Course with a Focus on Active Learning Through Integrated Curricular Approach: Pharmacy Care Laboratory I (1999) (6)
- A Dual Controlled Gastrointestinal Therapeutic System of Salmon Calcitonin. II. Screening of Process and Formulation Variables (2004) (6)
- Comparative evaluation of controlled-release solid oral dosage forms prepared with solid dispersions and coprecipitates (1999) (5)
- Preparation and characterization of dicarboxylic acids salt of aripiprazole with enhanced physicochemical properties (2021) (5)
- Studying effect of glyceryl palmitostearate amount, manufacturing method and stability on polymorphic transformation and dissolution of rifaximin tablets. (2020) (5)
- Artificial neural network and simplex optimization for mixing of aqueous-coated beads to obtain controlled-release formulations (2000) (5)
- Quantitative evaluation of the thallium binding of soluble and insoluble Prussian blue hexacyanoferrate analogs: A scientific comparison based on their critical quality attributes. (2019) (5)
- Application of chemometric methods to differential scanning calorimeter (DSC) to estimate nimodipine polymorphs from cosolvent system (2015) (4)
- CALCIUM PHOSPHATE IN PHARMACEUTICAL PRODUCT DEVELOPMENT (1998) (4)
- In-Use Stability Assessment of FDA Approved Metformin Immediate Release and Extended Release Products for N-Nitrosodimethylamine and Dissolution Quality Attributes. (2022) (4)
- Nanotechnology-based drug products (2018) (4)
- Stability characterization and appearance of particulates in a lyophilized formulation of a model peptide hormone-human secretin. (2015) (4)
- Preparation and in vitro characterization of self-nanoemulsified drug delivery systems of coenzyme Q10 using chiral essential oil components (2004) (4)
- Effects of Diluents on Physical and Chemical Stability of Phenytoin and Phenytoin Sodium (2020) (4)
- Semi‐fluorinated polyarylenes: Microwave‐assisted synthesis and structure–property relationships (2020) (4)
- To investigate the influence of machine operating variables on formulations derived from lactose types in capsule filling: part 2 (2016) (4)
- Solid phase extraction of Pb(II) and Cd(II) using reduced graphene oxide-polychloroprene impregnated with magnetic nanoparticle (MNPs-RGO-PCP) (2018) (4)
- The Science and Regulatory Perspectives of Emerging Controlled Release Dosage Forms (2010) (4)
- Univariate and multivariate models for determination of prasugrel base in the formulation of prasugrel hydrochloride using XRPD method. (2019) (4)
- Optimization and In Vivo Evaluation of an Oral Dual Controlled-Release Tablet Dosage Form of Insulin and Duck Ovomucoid (2008) (4)
- Magnetic solid phase extraction of Cd (II) using magnetic nanoparticle (MNPs) and silica coated magnetic nanoparticles (SiMNPs) from environmental water samples (2017) (3)
- Challenges and Opportunities for Biotech Quality by Design (2015) (3)
- Critical Importance and Quality Evaluation of Drug Delivery Autoinjectors in the FDA-DOD Shelf Life Extension Program (SLEP) (2016) (3)
- Spontaneous carbonate formation in an amorphous, amine-rich, polymeric drug substance: sevelamer HCl product quality. (2012) (3)
- Salt Engineering of Aripiprazole with Polycarboxylic Acids to Improve Physicochemical Properties (2021) (3)
- Fabrication of MNPs/rGO/PMMA Composite for the Removal of Hazardous Cr(VI) from Tannery Wastewater through Batch and Continuous Mode Adsorption (2021) (3)
- Elimination of Ni(II) from water samples using composite of magnetic nanoparticles orange peel (MNP-OP) (2020) (3)
- Development of Stable Amorphous Solid Dispersion and Quantification of Crystalline Fraction of Lopinavir by Spectroscopic-chemometric Methods. (2021) (3)
- HIV-1 Tat and cocaine impact astrocytic energy reservoir influence on miRNA epigenetic regulation. (2021) (3)
- Chemometric evaluation of brompheniramine-tannate complexes. (2012) (3)
- NIPTE-FDA Excipients Knowledge Base (2011) (3)
- Coating characterization by hyperspectroscopy and predictive dissolution models of tablets coated with blends of cellulose acetate and cellulose acetate phthalate (2021) (3)
- In-Situ Implant Formulation of Laurate and Myristate Prodrugs of Dolutegravir for Ultra-Long Delivery. (2022) (3)
- Permeation of genistein through human skin (2003) (3)
- An Enteric Dual‐Controlled Gastrointestinal Therapeutic System of Salmon Calcitonin‐I: Preparation, Characterization, and Preclinical Bioavailability in Rats (2004) (3)
- Development of a Multivariate Predictive Dissolution Model for Tablets Coated with Cellulose Ester Blends (2020) (2)
- FDA Analysis of Atorvastatin Products Refutes Report of Methyl Ester Impurities (2014) (2)
- Regulatory Issues and Challenges Associated with the Development of Performance Specifications for Modified Release Parenteral Products (2012) (2)
- Stability of Split Tablets (2010) (2)
- Use of SIRC Rabbit Corneal Cell Lines Grown on Polycarbonate- or Polyester-Based Filters to Assess the In Vitro Corneal Transport/Toxicity Screening Using Pilocarpine With or Without Benzalkonium Chloride (2003) (2)
- Dose uniformity of scored and unscored tablets: Application of the FDA Tablet Scoring Guidance for Industry. (2016) (2)
- A headspace-gas chromatography method for isopropanol determination in warfarin sodium products as a measure of drug crystallinity (2018) (2)
- Consistency of Pharmaceutical Products: An FDA Perspective on Hot-Melt Extrusion Process (2013) (2)
- Measurement Process Prospects using THz Spectroscopy for Pharmaceutical Applications (2005) (2)
- In Vitro Drug Transfer Due to Drug Retention in Human Epidermis Pretreated with Application of Marketed Estradiol Transdermal Systems (2017) (2)
- Regulatory Aspects of Freeze-Drying (2018) (2)
- Regulatory Perspective on the Development of Polymer Nanomaterials (2016) (2)
- Segmentation of Brain Tumor in Multimodal MRI using Histogram Differencing & KNN (2017) (2)
- Magnetic solid-phase extraction of Cd(II) from water samples using magnetic nanoparticles impregnated walnut shells powder (MNPS-WSP) (2021) (1)
- High Dose Vardenafil Blunts the Hypertensive Effects of Toll-Like Receptor 3 Activation During Pregnancy (2021) (1)
- Calculations Involving Suppositories (2000) (1)
- Stability of two concentrations of tiagabine in an extemporaneously compounded suspension. (2003) (1)
- EFFECTS OF SMOKELESS TOBACCO ON THE DEVELOPING LIVER OF THE MICE (2013) (1)
- Comparative solid phase extractions of Pb(II) from water samples using magnetic nanoparticles impregnated banana peels (MNPs-BP), magnetic nanoparticles (MNPs) and banana peels (BP) (2017) (1)
- Workshop Report: USP Workshop on Exploring the Science of Drug Absorption (2019) (1)
- Potential Application of USP Paddle and Basket Dissolution Methods in Discriminating for Portioned Moist Snuff and Snus Smokeless Tobacco Products (2021) (1)
- FDA: contribution to developing pediatric formulations and transatlantic collaboration. (2012) (1)
- Pediatric and Geriatric Dosing (2000) (1)
- Design Space Definition (2017) (1)
- Data integrity issues in pharmaceutical industry: Common observations, challenges and mitigations strategies. (2022) (1)
- Stability of Repackaged Products (2010) (1)
- Development and Validation of a Discriminatory Dissolution Method for Portioned Moist Snuff and Snus. (2021) (1)
- Using Terahertz Spectroscopy to Quantify Pharmaceutical Tablet Composition (2005) (1)
- Scientific and Regulatory Considerations in Product Development (2015) (1)
- Ion Gel Coated Graphene Field Effect Transistor for Humidity Sensing Applications (2021) (1)
- Formulation development and stability evaluation of a multicomponent nutritional supplement (2001) (1)
- Lyophilization of Biologics: An FDA Perspective (2015) (1)
- HIV-1 Tat and cocaine impact astrocytic energy reservoirs and epigenetic regulation by influencing the LINC01133-hsa-miR-4726-5p-NDUFA9 axis (2022) (1)
- HIV-1 Tat and cocaine coexposure impacts piRNAs to affect astrocyte energy metabolism. (2022) (1)
- Useful Clinical Formulae (2000) (0)
- Development of Abuse-Deterrent Formulations Using Sucrose Acetate Isobutyrate (2020) (0)
- Calculations Involving Injectable Medications (2000) (0)
- Crystallization Systems (2016) (0)
- Potential Application of USP Paddle and Basket Dissolution Methods in Discriminating for Portioned Moist Snuff and Snus Smokeless Tobacco Products (2021) (0)
- Critical Importance and Quality Evaluation of Drug Delivery Autoinjectors in the FDA-DOD Shelf Life Extension Program (SLEP) (2016) (0)
- Answers to Practice Problems (2000) (0)
- Prerequisite Mathematics Review (2000) (0)
- Understanding Pharmaceutical Quality by Design Citation (2014) (0)
- Use of In Vitro–In Vivo Correlation to Predict the Pharmacokinetics of Several Products Containing a BCS Class 1 Drug in Extended Release Matrices (2012) (0)
- Moderating Effect of Market Environment on the Relationship of Corporate Social Responsibility and Firm Performance of Banking Sector in Pakistan (2021) (0)
- Quality-byDesign ( QbD ) Case Study : Powder Blending Process Kinetics Evaluation (2008) (0)
- Improvement of Physicochemical Properties of an Antiepileptic Drug by Salt Engineering (2012) (0)
- Preparation and Characterization of Stable Amorphous Glassy Solution of BCS II and IV Drugs (2021) (0)
- In Vitro Drug Transfer Due to Drug Retention in Human Epidermis Pretreated with Application of Marketed Estradiol Transdermal Systems (2016) (0)
- A Study On Thyroxine and Thyroid Stimulating Hormone in Women During Pregnancy (1999) (0)
- ALENDRONATE A PROMISING / MULTI ASPECT DRUG IN THE MANAGEMENT OF OSTOEOPOROSIS (2011) (0)
- Formulation Characterization and Pharmacokinetic Evaluation of Amorphous Solid Dispersions of Dasatinib (2022) (0)
- Calculations Involving Immunizing Agents and Vaccines (2000) (0)
- Calculations Involving Nutrition (2000) (0)
- Pyrimethamine 3D printlets for pediatric toxoplasmosis: design, pharmacokinetics, and anti-toxoplasma activity (2023) (0)
- Quality-by-Design (QbD) for Capsule Formulation and Process Development : Regulatory Science Relevance, Scientific Case Studies, and Future Challenges 1 (2017) (0)
- Calculations Involving Capsules, Tablets, and Powder Dosage Forms (2000) (0)
- A Comparative Evaluation of Polystyrene Divinylbenzene Copolymer HPLC Columns on the Chromatographic Performance of the Compendial Method for Doxycycline Hyclate Capsules: Implications for Method Implementation of a Medical Countermeasure Medication (2015) (0)
- Scientific and Regulatory Overview of Process Analytical Technology in Bioprocesses (2011) (0)
- Engineering Considerations on Modeling for Pharmaceutical Process Analytical Technology ( PAT ) Applications (2006) (0)
- Quality-by-Design (QbD) for Capsule Formulation and Process Development: Regulatory Science Relevance, Scientific Case Studies, and Future Challenges (2017) (0)
- The Science and Regulatory Perspectives of Pharmaceutical Suspensions (2010) (0)
- Quality by Design and Control Strategies for Parenteral Dosage Forms (2019) (0)
- Physicochemical Characterization of Complex Drug Substances: Evaluation of Structural Similarities and Differences of Protamine Sulfate from Various Sources (2012) (0)
- Development and Validation of a HPLC Method for Dissolution and Stability Assay of Liquid-Filled Cyclosporine Capsule Drug Products (2013) (0)
- Effects of Diluents on Physical and Chemical Stability of Phenytoin and Phenytoin Sodium (2020) (0)
- Calculations Involving Ointments, Creams, and Other Semisolids (2000) (0)
- Nitroso Impurities in Drug Products: An Overview of Risk Assessment, Regulatory Milieu, and Control Strategy (2023) (0)
- Development, assessment and stability studies of Naloxone hydrochloride sublingual drug delivery system (2016) (0)
- Salt Engineering of Aripiprazole with Polycarboxylic Acids to Improve Physicochemical Properties (2021) (0)
- Answers to Review Problems (2000) (0)
- A spectrophotometric Study of the Association of Nickel with taurine (1965) (0)
- In Vitro and In Vivo Characterization of the Transdermal Gel Formulation of Desloratadine for Prevention of Obesity and Metabolic Syndrome (2023) (0)
- Formulation and Route of Administration—Influencing Drug Permeability and Absorption (2005) (0)
- Scientific and regulatory challenges of bioavailability/ bioequivalence in the 21st century (2010) (0)
- Calculation of Doses and Dose Adjustments (2000) (0)
- Defining Patient Centric Pharmaceutical Drug Product Design (2016) (0)
- RESPONSE OF THE ADULT FEMALE RATS TO OVARIECTOMY AS DETERMINED BY LUTEINISING HORMONE RADIOIMMUNOASSAY (1998) (0)
- Comparison of Univariate and Multivariate Models of 13C SSNMR and XRPD Techniques for Quantification of Nimodipine Polymorphs (2015) (0)
- Liposome Formation Using a Coaxial Turbulent Jet in Co-Flow (2015) (0)
This paper list is powered by the following services:
What Schools Are Affiliated With Mansoor Khan?
Mansoor Khan is affiliated with the following schools:
