A. Siddiqui

发表

Chemometric methods for the quantification of crystalline tacrolimus in solid dispersion by powder X-ray diffractrometry.

M. Khan, A. Siddiqui, Ziyaur Rahman, 2014, Journal of pharmaceutical sciences.

Measurement of surface color as an expedient QC method for the detection of deviations in tablet hardness.

A. Siddiqui, S. Nazzal, 2007, International journal of pharmaceutics.

Characterization of a nonribosomal peptide antibiotic solid dispersion formulation by process analytical technologies sensors.

M. Khan, A. Siddiqui, Ziyaur Rahman, 2013, Journal of pharmaceutical sciences.

Evaluation of Abuse-Deterrent Characteristics of Tablets Prepared via Hot-Melt Extrusion

M. Khan, A. Siddiqui, Ziyaur Rahman, 2019, AAPS PharmSciTech.

Root cause evaluation of particulates in the lyophilized indomethacin sodium trihydrate plug for parenteral administration.

M. Khan, D. Awotwe-Otoo, A. Siddiqui, 2014, International journal of pharmaceutics.

Chemometric evaluation of near infrared, fourier transform infrared, and Raman spectroscopic models for the prediction of nimodipine polymorphs.

M. Khan, A. Siddiqui, Ziyaur Rahman, 2013, Journal of pharmaceutical sciences.

Modeling the effect of sonication parameters on size and dispersion temperature of solid lipid nanoparticles (SLNs) by response surface methodology (RSM)

A. Siddiqui, S. Nazzal, A. Alayoubi, 2014, Pharmaceutical development and technology.

Understanding effect of formulation and manufacturing variables on the critical quality attributes of warfarin sodium product.

M. Khan, A. Siddiqui, Ziyaur Rahman, 2015, International journal of pharmaceutics.

Assessing impact of formulation and process variables on in-vitro performance of directly compressed abuse deterrent formulations.

M. Khan, A. Siddiqui, Ziyaur Rahman, 2016, International journal of pharmaceutics.

The effect of emulsifying wax on the physical properties of CTAB-based solid lipid nanoparticles (SLN)

A. Siddiqui, S. Nazzal, A. Alayoubi, 2014, Pharmaceutical development and technology.

Application of NIR chemometric methods for quantification of the crystalline fraction of warfarin sodium in drug product

M. Khan, S. Akhtar, A. Siddiqui, 2016, Drug development and industrial pharmacy.

Powdered self-emulsified lipid formulations of meloxicam as solid dosage forms for oral administration

A. Siddiqui, S. Nazzal, A. Alayoubi, 2013, Drug development and industrial pharmacy.

Application of Optical Coherence Tomography Freeze-Drying Microscopy for Designing Lyophilization Process and Its Impact on Process Efficiency and Product Quality

Celia N. Cruz, D. Awotwe-Otoo, A. Siddiqui, 2017, AAPS PharmSciTech.

Development and Validation of Sample Preparation and an HPLC Analytical Method for Dissolution Testing in Fed-State Simulated Gastric Fluid—Illustrating Its Application for Ibuprofen and Ketoconazole Immediate Release Tablets

K. Morris, A. Siddiqui, A. Selen, 2020, AAPS PharmSciTech.

Doxorubicin and MBO-asGCS oligonucleotide loaded lipid nanoparticles overcome multidrug resistance in adriamycin resistant ovarian cancer cells (NCI/ADR-RES).

A. Siddiqui, S. Nazzal, Vineet Gupta, 2012, International journal of pharmaceutics.

Mixed backbone antisense glucosylceramide synthase oligonucleotide (MBO-asGCS) loaded solid lipid nanoparticles: in vitro characterization and reversal of multidrug resistance in NCI/ADR-RES cells.

A. Siddiqui, S. Nazzal, G. Patwardhan, 2010, International journal of pharmaceutics.

Oseltamivir phosphate-amberlite(TM) IRP 64 ionic complex for taste masking: preparation and chemometric evaluation.

M. Khan, R. Shah, A. Siddiqui, 2013, Journal of pharmaceutical sciences.

Evaluation of Abuse-Deterrent Characteristics of Tablets Prepared via Hot-Melt Extrusion

A. Siddiqui, Ziyaur Rahman, Charudharshini Srinivasan, 2019, AAPS PharmSciTech.

The Effect of Media Composition, pH, and Formulation Excipients on the In Vitro Lipolysis of Self-Emulsifying Drug Delivery Systems (SEDDS)

A. Siddiqui, S. Nazzal, H. Ali, 2010 .

Dissolution and powder flow characterization of solid self-emulsified drug delivery system (SEDDS).

Akhtar Siddiqui, Vikas Agarwal, Hazem Ali, 2009, International journal of pharmaceutics.

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.

M. Khan, S. Akhtar, A. Siddiqui, 2015, Journal of pharmaceutical sciences.

Orally disintegrating tablet of novel salt of antiepileptic drug: formulation strategy and evaluation.

Ziyaur Rahman, Akhtar Siddiqui, M. Khan, 2013, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Effects of excipients and curing process on the abuse deterrent properties of directly compressed tablets.

Celia N. Cruz, M. Khan, A. Siddiqui, 2017, International journal of pharmaceutics.

Regulatory Considerations in Development of Amorphous Solid Dispersions

Abhay Gupta, Mansoor A. Khan, Ziyaur Rahman, 2014 .

Impact of formulation and process variables on solid-state stability of theophylline in controlled release formulations.

M. Khan, A. Siddiqui, Ziyaur Rahman, 2016, International journal of pharmaceutics.

A method for the tribological assessment of oral pharmaceutical liquids

R. G. Hollenbeck, S. Hoag, A. Siddiqui, 2022, Drug development and industrial pharmacy.

Application of chemometric methods to differential scanning calorimeter (DSC) to estimate nimodipine polymorphs from cosolvent system

M. Khan, A. Siddiqui, Ziyaur Rahman, 2015, Drug development and industrial pharmacy.

Assessing the impact of nimodipine devitrification in the ternary cosolvent system through quality by design approach.

Ziyaur Rahman, Akhtar Siddiqui, M. Khan, 2013, International journal of pharmaceutics.

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.

M. Khan, A. Siddiqui, Ziyaur Rahman, 2015, Journal of pharmaceutical sciences.

K. Morris, A. Siddiqui, A. Selen, 2020, AAPS PharmSciTech.

Determination of tacrolimus crystalline fraction in the commercial immediate release amorphous solid dispersion products by a standardized X-ray powder diffraction method with chemometrics.

M. Khan, A. Siddiqui, Ziyaur Rahman, 2014, International journal of pharmaceutics.

Comparison of Univariate and Multivariate Models of 13C SSNMR and XRPD Techniques for Quantification of Nimodipine Polymorphs

M. Khan, A. Siddiqui, Ziyaur Rahman, 2015, AAPS PharmSciTech.

Evaluation of In-Use Stability of Anticoagulant Drug Products: Warfarin Sodium.

M. Khan, S. Akhtar, A. Siddiqui, 2015, Journal of Pharmacy and Science.

A headspace-gas chromatography method for isopropanol determination in warfarin sodium products as a measure of drug crystallinity

M. Khan, S. Akhtar, A. Siddiqui, 2018, Acta pharmaceutica.

Development and validation of X-ray diffraction method for quantitative determination of crystallinity in warfarin sodium products.

M. Khan, A. Siddiqui, Ziyaur Rahman, 2015, International journal of pharmaceutics.

Near-infrared and fourier transform infrared chemometric methods for the quantification of crystalline tacrolimus from sustained-release amorphous solid dispersion.

M. Khan, A. Siddiqui, Ziyaur Rahman, 2014, Journal of pharmaceutical sciences.

Stability characterization and appearance of particulates in a lyophilized formulation of a model peptide hormone-human secretin.

M. Khan, A. Siddiqui, Charudharshini Srinivasan, 2015, International journal of pharmaceutics.

Dissolution and powder flow characterization of solid self-emulsified drug delivery system (SEDDS).

A. Siddiqui, S. Nazzal, V. Agarwal, 2009, International journal of pharmaceutics.

An analysis of the swimming problem of a singly flagellated micro-organism in an MHD fluid flowing through a porous medium

T. Hayat, A. Siddiqui, A. Ansari, 2010 .