Bioavailability enhancement of poorly water-soluble drugs via nanocomposites: Formulation–Processing aspects and challenges

A Bhakay, M Rahman, RN Dave, E Bilgili - Pharmaceutics, 2018 - mdpi.com
Drug nanoparticles embedded in a dispersant matrix as a secondary phase, ie, drug-laden
nanocomposites, offer a versatile delivery platform for enhancing the dissolution rate and …

Nanomilling of drugs for bioavailability enhancement: a holistic formulation-process perspective

M Li, M Azad, R Davé, E Bilgili - Pharmaceutics, 2016 - mdpi.com
Preparation of drug nanoparticles via wet media milling (nanomilling) is a very versatile drug
delivery platform and is suitable for oral, injectable, inhalable, and buccal applications. Wet …

Engineered nanocrystal technology: in-vivo fate, targeting and applications in drug delivery

VK Pawar, Y Singh, JG Meher, S Gupta… - Journal of Controlled …, 2014 - Elsevier
Abstract Formulation of nanocrystals is a robust approach which can improve delivery of
poorly water soluble drugs, a challenge pharmaceutical industry has been facing since long …

Nanosuspensions of poorly water-soluble drugs prepared by bottom-up technologies

J Du, X Li, H Zhao, Y Zhou, L Wang, S Tian… - International journal of …, 2015 - Elsevier
In recent years, nanosuspension has been considered effective in the delivery of water-
soluble drugs. One of the main challenges to effective drug delivery is designing an …

Formulation aspects of intravenous nanosuspensions

D Patel, SS Zode, AK Bansal - International Journal of Pharmaceutics, 2020 - Elsevier
Intravenous (IV) route is preferred for rapid onset of action, avoiding first pass metabolism
and achieving site specific delivery. Development of IV formulations for poorly water soluble …

Formation of nanosuspensions in bottom-up approach: theories and optimization

A Ahmadi Tehrani, MM Omranpoor, A Vatanara… - DARU Journal of …, 2019 - Springer
Background Nanosuspensions, liquid dispersions with nanometer size distribution, are
becoming trendy in pharmaceutical practice to formulate poorly water-soluble drugs and to …

Impact of nanosizing on solubility and dissolution rate of poorly soluble pharmaceuticals

SB Murdande, DA Shah, RH Dave - Journal of pharmaceutical sciences, 2015 - Elsevier
The quantitative determination of solubility and the initial dissolution rate enhancement of
crystalline nanoparticles were critically investigated using a separation-based approach …

Solidification of nanosuspensions for the production of solid oral dosage forms and inhalable dry powders

M Malamatari, S Somavarapu, KMG Taylor… - Expert opinion on …, 2016 - Taylor & Francis
Introduction: Nanosuspensions combine the advantages of nanotherapeutics (eg increased
dissolution rate and saturation solubility) with ease of commercialisation. Transformation of …

Risk assessment and QbD based optimization of an Eprosartan mesylate nanosuspension: In-vitro characterization, PAMPA and in-vivo assessment

P Shekhawat, V Pokharkar - International journal of pharmaceutics, 2019 - Elsevier
Quality by design (QbD) principles were implemented to understand the product and
process variables of sonoprecipitation technique, for preparation of eprosartan mesylate …

[HTML][HTML] Freeze-drying of drug nanosuspension–study of formulation and processing factors for the optimization and characterization of redispersible cilostazol …

E Jakubowska, M Bielejewski, B Milanowski… - Journal of Drug Delivery …, 2022 - Elsevier
The aim of this work was to systematically study the effect of freeze-drying of bottom-up
processed cilostazol nanosuspension on the particle size after redispersion. Several …