Controversies with self-emulsifying drug delivery system from pharmacokinetic point of view
B Chatterjee, S Hamed Almurisi… - Drug …, 2016 - Taylor & Francis
Self-emulsifying drug delivery system (SEDDS) is an isotropic mixture of lipid, surfactant and
co-surfactant, which forms a fine emulsion when comes in contact of an aqueous medium …
co-surfactant, which forms a fine emulsion when comes in contact of an aqueous medium …
Mucoadhesive polymers and their mode of action: A recent update
B Chatterjee, N Amalina, P Sengupta… - Journal of Applied …, 2017 - japsonline.com
The potential of mucoadhesive delivery system for sustained delivery of drug has been
established few decades back. Different polymeric systems such as single or combined …
established few decades back. Different polymeric systems such as single or combined …
Injectable systems of chitosan in situ forming composite gel incorporating linezolid-loaded biodegradable nanoparticles for long-term treatment of bone infections
The objective of the current study was to create an efficient, minimally invasive combined
system comprising in situ forming hydrogel loaded with both spray-dried polymeric …
system comprising in situ forming hydrogel loaded with both spray-dried polymeric …
[HTML][HTML] Structural characteristics, binding behaviors, and stability of ternary nanocomplexes of lecithin, polyvinylpyrrolidone, and curcumin
QQ Yang, WQ Cai, ZX Wang, Y Li, Y Zhang, X Lin… - Lwt, 2023 - Elsevier
Low stability and bioaccessibility are two unfavourable features that limit the application of
many hydrophobic compounds. In this study, lecithin was complexed with …
many hydrophobic compounds. In this study, lecithin was complexed with …
Amorphization of drugs for transdermal delivery-a recent update
B Chatterjee, A Reddy, M Santra, S Khamanga - Pharmaceutics, 2022 - mdpi.com
Amorphous solid dispersion is a popular formulation approach for orally administered poorly
water-soluble drugs, especially for BCS class II. But oral delivery could not be an automatic …
water-soluble drugs, especially for BCS class II. But oral delivery could not be an automatic …
[HTML][HTML] Drug crystal growth in ternary amorphous solid dispersions: Effect of surfactants and polymeric matrix-carriers
The present study evaluates the crystal growth rate of amorphous drugs when dispersed in
different ternary polymeric amorphous solid dispersions (ASDs) in the presence of …
different ternary polymeric amorphous solid dispersions (ASDs) in the presence of …
Self-microemulsifying drug-delivery system: ongoing challenges and future ahead
Self-microemulsifying drug-delivery system (SMEDDS) can be defined as an isotropic
system containing lipid and surfactant as well as cosurfactant that develop an emulsion in …
system containing lipid and surfactant as well as cosurfactant that develop an emulsion in …
Quality by design–based development and optimization of fourth-generation ternary solid dispersion of standardized Piper longum extract for melanoma therapy
The study aimed to enhance the solubility, dissolution, and oral bioavailability of
standardized Piper longum fruits ethanolic extract (PLFEE) via fourth-generation ternary …
standardized Piper longum fruits ethanolic extract (PLFEE) via fourth-generation ternary …
Curcumin-loaded self-nanomicellizing solid dispersion system: Part I: Development, optimization, characterization, and oral bioavailability
Curcumin (CUR) is considered as one of the most bioactive molecules ever discovered from
nature due to its proven anti-inflammatory and antioxidant in both preclinical and clinical …
nature due to its proven anti-inflammatory and antioxidant in both preclinical and clinical …
Optimization of aceclofenac proniosomes by using different carriers, part 1: Development and characterization
In the contemporary medical model world, the proniosomal system has been serving as a
new drug delivery system that is considered to significantly enhance the bioavailability of …
new drug delivery system that is considered to significantly enhance the bioavailability of …