[PDF][PDF] Pharmaceutical Cocrystals: An Overview.
Poor aqueous solubility and low oral bioavailability of an active pharmaceutical ingredient
are the major constraints during the development of new product. Various approaches have …
are the major constraints during the development of new product. Various approaches have …
The Biopharmaceutics Classification System: subclasses for in vivo predictive dissolution (IPD) methodology and IVIVC
Y Tsume, DM Mudie, P Langguth, GE Amidon… - European Journal of …, 2014 - Elsevier
Abstract The Biopharmaceutics Classification System (BCS) has found widespread utility in
drug discovery, product development and drug product regulatory sciences. The …
drug discovery, product development and drug product regulatory sciences. The …
Pharmaceutical co-crystals: A green way to enhance drug stability and solubility for improved therapeutic efficacy
A Chettri, A Subba, GP Singh… - Journal of Pharmacy and …, 2024 - academic.oup.com
Pharmaceutical co-crystals have gained significant attention in recent years as a promising
green and sustainable method for poorly soluble drugs to improve their solubility, stability …
green and sustainable method for poorly soluble drugs to improve their solubility, stability …
RETRACTED ARTICLE: Berberine nanoparticles with enhanced in vitro bioavailability: characterization and antimicrobial activity
MUK Sahibzada, A Sadiq, HS Faidah… - Drug design …, 2018 - Taylor & Francis
Sahibzada MUK, Sadiq A, Faidah HS, et al. Drug Des Devel Ther. 2018; 12: 303–312. We,
the Editors and Publisher of Drug Design, Development and Therapy, have retracted the …
the Editors and Publisher of Drug Design, Development and Therapy, have retracted the …
[HTML][HTML] Co-crystals: a novel approach to modify physicochemical properties of active pharmaceutical ingredients
AV Yadav, AS Shete, AP Dabke… - Indian journal of …, 2009 - ncbi.nlm.nih.gov
Crystal form can be crucial to the performance of a dosage form. This is especially true for
compounds that have intrinsic barriers to drug delivery, such as low aqueous solubility, slow …
compounds that have intrinsic barriers to drug delivery, such as low aqueous solubility, slow …
Development and evaluation of sunscreen creams containing morin-encapsulated nanoparticles for enhanced UV radiation protection and antioxidant activity
The objective of present work was to develop novel sunscreen creams containing polymeric
nanoparticles (NPs) of morin. Polymeric NPs containing morin were prepared and …
nanoparticles (NPs) of morin. Polymeric NPs containing morin were prepared and …
In silico prediction of drug dissolution and absorption with variation in intestinal pH for BCS class II weak acid drugs: ibuprofen and ketoprofen
Y Tsume, P Langguth, A Garcia‐Arieta… - … & drug disposition, 2012 - Wiley Online Library
ABSTRACT The FDA Biopharmaceutical Classification System guidance allows waivers for
in vivo bioavailability and bioequivalence studies for immediate‐release solid oral dosage …
in vivo bioavailability and bioequivalence studies for immediate‐release solid oral dosage …
Dissolution-modulating mechanism of alkalizers and polymers in a nanoemulsifying solid dispersion containing ionizable and poorly water-soluble drug
TTD Tran, PHL Tran, BJ Lee - European Journal of Pharmaceutics and …, 2009 - Elsevier
We investigated the dissolution-modulating mechanism of alkalizers and polymers in
nanoemulsifying Gelucire 44/14 (GUC)-based solid dispersions (SDs) for controlled release …
nanoemulsifying Gelucire 44/14 (GUC)-based solid dispersions (SDs) for controlled release …
[PDF][PDF] Dissolution improvement of simvastatin by surface solid dispersion technology
The objective of the present study was to formulate surface solid dispersions (SSD) of
simvastatin to improve the aqueous solubility and dissolution rate to facilitate faster onset of …
simvastatin to improve the aqueous solubility and dissolution rate to facilitate faster onset of …
Formulation and characterization of aceclofenac-loaded nanofiber based orally dissolving webs
Aceclofenac-loaded poly (vinyl-pyrrolidone)-based nanofiber formulations were prepared by
electrospinning to obtain drug-loaded orally disintegrating webs to enhance the solubility …
electrospinning to obtain drug-loaded orally disintegrating webs to enhance the solubility …