Advances in coamorphous drug delivery systems☆

Autor: Qin Shi, Sakib M. Moinuddin, Ting Cai
Jazyk: angličtina
Rok vydání: 2018
Předmět:
Drug
AUC
area under plasma concentrations-time curve

Bioavailability
TGA
thermogravimetric analysis

media_common.quotation_subject
SEM
scanning electron microscope

Characterization
Nanotechnology
Review
IDR
intrinsic dissolution rate

NMR - Nuclear magnetic resonance
Cmax
maximum plasma concentration

03 medical and health sciences
0302 clinical medicine
DSC
differential scanning calorimetry

MTDSC
modulated temperature differential scanning calorimetry

Dc
relative degree of crystallization

P-gp
P-glycoprotein

General Pharmacology
Toxicology and Pharmaceutics

NMR
nuclear magnetic resonance

LLPS
liquid—liquid phase separation

Tg
glass transition temperature

030304 developmental biology
media_common
Coamorphous
Active ingredient
LFRS
low-frequency Raman spectroscopy

0303 health sciences
Physical stability
Chemistry
RH
relative humidity

lcsh:RM1-950
DVS
dynamic vapor sorption

PXRD
powder X-ray diffraction

BCS
bio-pharmaceutics classification systems

API
active pharmaceutical ingredient

UV
ultraviolet spectroscopy

lcsh:Therapeutics. Pharmacology
Css
plasma concentration at steady state

HPLC
high performance liquid chromatography

030220 oncology & carcinogenesis
Drug delivery
Preparation
FT-IR
fourier transform infrared spectroscopy

HME
hot melt extrusion

Dissolution
Tmax
time of maximum plasma concentration
Zdroj: Acta Pharmaceutica Sinica. B
Acta Pharmaceutica Sinica B, Vol 9, Iss 1, Pp 19-35 (2019)
ISSN: 2211-3843
2211-3835
Popis: In recent years, the coamorphous drug delivery system has been established as a promising formulation approach for delivering poorly water-soluble drugs. The coamorphous solid is a single-phase system containing an active pharmaceutical ingredient (API) and other low molecular weight molecules that might be pharmacologically relevant APIs or excipients. These formulations exhibit considerable advantages over neat crystalline or amorphous material, including improved physical stability, dissolution profiles, and potentially enhanced therapeutic efficacy. This review provides a comprehensive overview of coamorphous drug delivery systems from the perspectives of preparation, physicochemical characteristics, physical stability, in vitro and in vivo performance. Furthermore, the challenges and strategies in developing robust coamorphous drug products of high quality and performance are briefly discussed.
Graphical abstract fx1
Databáze: OpenAIRE