Liposil, a promising composite material for drug storage and release

S Bégu, AA Pouëssel, DA Lerner… - Journal of controlled …, 2007 - Elsevier
Preliminary tests in the field of drug storage and release of composite materials known as
liposils were described. These silica-based particles were obtained via liposome templating …

Nimesulide PLA microspheres as a potential sustained release system for the treatment of inflammatory diseases

MN Freitas, JM Marchetti - International journal of pharmaceutics, 2005 - Elsevier
Polylactic acid (PLA-l) microspheres were prepared as a biodegradable polymeric carrier for
a non-steroidal anti-inflammatory drug, nimesulide. The preparation of this system was …

Encapsulation of liposomes within pH responsive microspheres for oral colonic drug delivery

MJ Barea, MJ Jenkins, YS Lee… - International journal …, 2012 - Wiley Online Library
A novel liposome‐in‐microsphere (LIM) formulation has been created comprising drug‐
loaded liposomes within pH responsive Eudragit S100 microspheres. The liposomes …

Amorphous salts solid dispersions of celecoxib: enhanced biopharmaceutical performance and physical stability

S Mukesh, P Joshi, AK Bansal… - Molecular …, 2021 - ACS Publications
Numerous amorphous solid dispersion (ASD) formulations of celecoxib (CEL) have been
attempted for enhancing the solubility, dissolution rate, and in vivo pharmacokinetics via …

Challenges and opportunities in the encapsulation of liquid and semi-solid formulations into capsules for oral administration

ET Cole, D Cadé, H Benameur - Advanced drug delivery reviews, 2008 - Elsevier
The encapsulation of liquids and semi-solids provides solutions for convenient delivery
through improved oral absorption of poorly water-soluble drugs. In addition, low dose …

Formulation and characterization of lipid-based drug delivery system of raloxifene-microemulsion and self-microemulsifying drug delivery system

H Thakkar, J Nangesh, M Parmar… - Journal of Pharmacy and …, 2011 - journals.lww.com
Background: Raloxifene, a second-generation selective estrogen receptor modulator
(SERM) used to prevent osteoporosis in postmenopausal women is administered orally in …

Recent advances in lipid nanoparticle formulations with solid matrix for oral drug delivery

S Das, A Chaudhury - Aaps Pharmscitech, 2011 - Springer
Lipid nanoparticles based on solid matrix have emerged as potential drug carriers to
improve gastrointestinal (GI) absorption and oral bioavailability of several drugs, especially …

[HTML][HTML] Mechanistic insights into effect of surfactants on oral bioavailability of amorphous solid dispersions

A Schittny, S Philipp-Bauer, P Detampel… - Journal of controlled …, 2020 - Elsevier
Drug delivery of poorly soluble drugs in form amorphous solid dispersions (ASDs) is an
appealing method to increase in vivo bioavailability. For rational formulation design, a …

[PDF][PDF] Encapsulation of water-insoluble drugs in polymer capsules prepared using mesoporous silica templates for intracellular drug delivery

Y Wang, Y Yan, J Cui, L Hosta-Rigau… - Adv …, 2010 - minerva-access.unimelb.edu.au
More than 40% of active compounds identified through screening of combinatorial libraries
are poorly water-soluble, rendering them unsuitable for further drug development because …

Solid lipid microparticles: formulation, preparation, characterisation, drug release and applications

S Jaspart, G Piel, L Delattre, B Evrard - Expert opinion on drug …, 2005 - Taylor & Francis
This review details the properties of solid lipid microparticles (SLMs): a promising drug
carrier system that has been until now rather unexploited. First, the advantages of SLMs …