Phenolic glycosides of the Salicaceae and their role as anti-herbivore defenses

GA Boeckler, J Gershenzon, SB Unsicker - Phytochemistry, 2011 - Elsevier
Since the 19th century the phytochemistry of the Salicaceae has been systematically
investigated, initially for pharmaceutical and later for ecological reasons. The result of these …

Amorphous drug delivery systems: molecular aspects, design, and performance

AM Kaushal, P Gupta, AK Bansal - Critical Reviews™ in …, 2004 - dl.begellhouse.com
The biopharmaceutical properties—especially the solubility and permeability—of a molecule
contribute to its overall therapeutic efficacy. The newer tools of drug discovery have caused …

Polymorphism in pharmaceutical solids

HG Brittain - Drugs and the pharmaceutical sciences, 1999 - api.taylorfrancis.com
It is now just about 10 years since the publication of the first edition of Polymorphism in
Pharmaceutical Solids, which certainly received a positive reaction from workers in drug …

Physics of amorphous solids

LR Hilden, KR Morris - Journal of pharmaceutical sciences, 2004 - Elsevier
The physical state of a dosage form, crystalline versus amorphous, is critical in determining
its solid‐state physical and chemical properties. This minireview describes the physics …

Processing of spherical crystalline particles via a novel solution atomization and crystallization by sonication (SAXS) technique

JS Kaerger, R Price - Pharmaceutical research, 2004 - Springer
Purpose. The objective was to develop a single-step pharmaceutical particle engineering
technique able to produce particles within a well-defined particle size range while …

Polymorphic form of piroxicam influences the performance of amorphous material prepared by ball-milling

K Naelapää, JP Boetker, P Veski, J Rantanen… - International journal of …, 2012 - Elsevier
The objective of this study was to investigate the influence of the starting solid state form of
piroxicam (anhydrate form I: PRXAH I vs form II: PRXAH II) on the properties of the resulting …

Influence of solid phase and formulation processing on stability of Abbott‐232 tablet formulations

J Wardrop, D Law, Y Qiu, K Engh… - Journal of …, 2006 - Wiley Online Library
Abbott‐232 is a chemically stable, highly water soluble non‐hygroscopic compound
selected for development as a potent uroselective α1A agonist. An anhydrate, a …

Stability challenges of amorphous solid dispersions of drugs: A critical review on mechanistic aspects

M Pisay, S Padya, S Mutalik… - Critical Reviews™ in …, 2024 - dl.begellhouse.com
The most common drawback of the existing and novel drug molecules is their low
bioavailability because of their low solubility. One of the most important approaches to …

[HTML][HTML] General Commentary: A Tribute to Professor Kenneth R. Morris–Scientist, Teacher, Mentor, Friend… and Underappreciated Academic Arborist

PLD Wildfong - Pharmaceutical Research, 2023 - Springer
This special issue of Pharmaceutical Research is dedicated to Professor Kenneth R. Morris,
who for more than 3 decades has been a leader in research devoted to the interplay …

Time-dependence of molecular mobility during structural relaxation and its impact on organic amorphous solids: an investigation based on a calorimetric approach

C Mao, SP Chamarthy, R Pinal - Pharmaceutical research, 2006 - Springer
Purpose To develop a calorimetry-based model for estimating the time-dependence of
molecular mobility during the isothermal relaxation of amorphous organic compounds below …