Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Sandip Gite"'
Publikováno v:
Current Drug Delivery. 18:1314-1329
Introduction: Surface engineering of nanocrystals for improving the biopharmaceutical features is a multivariate process involving numerous formulation and process variables, thus making it a complicated process to get the desired biopharmaceutical q
Publikováno v:
Drug Development and Industrial Pharmacy. 46:1763-1775
The article focuses on exploring and comparing two top-down methods, i.e. media milling and microfluidization for the fabrication of nanocrystals of rifampicin (RIF), a poorly water-soluble drug in terms of their potential for generation of stable an
Publikováno v:
AAPS PharmSciTech. 23(6)
The aim of this research was to develop a nanosuspension of aprepitant (APT) using the Nano-by-Design approach. A novel microfluidization technology was used for processing the formulation. A 3
Publikováno v:
Analytical Chemistry Letters. 8:587-600
Publikováno v:
Current drug delivery. 17(2)
Objective: The present study reports the use of MicrofluidizerTM technology to form a stable nanosuspension of atovaquone (ATQ) using quality by design (QbD) approach. Methods: The patient-centric quality target product profile and critical quality a
Publikováno v:
Dissolution Technologies. 23:14-20
Atorvastatin, an HMG CoA reductase inhibitor, is widely used for the treatment of dyslipidemia and prevention of cardiovascular disease. It belongs to Class 2 of the Biopharmaceutics Classification System owing to its low solubility and high permeabi
Autor:
Sandip Gite, Vandana B. Patravale
Publikováno v:
Journal of chromatographic science. 53(10)
A stability-indicating high-performance liquid chromatography (HPLC) procedure was developed for the determination of metformin HCl (MTH), atorvastatin calcium (AC) and glimepiride (GP) in combination and their main degradation products. The separati
Publikováno v:
Journal of chromatographic science. 52(4)
A sensitive, stability-indicating reversed-phase high-performance liquid chromatographic method was developed for the determination of eszopiclone and related impurities in tablet dosage form. The chromatographic separation was achieved on an Inertsi
Autor:
Gite, Sandip1, Patravale, Vandana1 vbp_muict@yahoo.co.in
Publikováno v:
Journal of Chromatographic Science. Nov/Dec2015, Vol. 53 Issue 10, p1654-1662. 9p.
Publikováno v:
Drug Development & Industrial Pharmacy. Nov2020, Vol. 46 Issue 11, p1763-1775. 13p.