Bioavailability of seocalcitol II: development and characterisation of self-microemulsifying drug delivery systems (SMEDDS) for oral administration containing medium and long chain triglycerides.
about
Pharmacokinetic aspects and in vitro-in vivo correlation potential for lipid-based formulationsMicroemulsions for oral administration and their therapeutic applicationsDevelopment of silymarin self-microemulsifying drug delivery system with enhanced oral bioavailabilityIn situ formation of nanocrystals from a self-microemulsifying drug delivery system to enhance oral bioavailability of fenofibrate.Role of medium-chain fatty acids in the emulsification mechanistics of self-micro-emulsifying lipid formulationsA Self-microemulsifying Drug Delivery System (SMEDDS) for a Novel Medicative Compound Against Depression: a Preparation and Bioavailability Study in Rats.Preparation and evaluation of self-nanoemulsifying tablets of carvedilol.New perspectives on lipid and surfactant based drug delivery systems for oral delivery of poorly soluble drugs.Role of excipients in successful development of self-emulsifying/microemulsifying drug delivery system (SEDDS/SMEDDS).Lipid-based nanosystem of edaravone: development, optimization, characterization and in vitro/in vivo evaluation.Rice germ oil as multifunctional excipient in preparation of self-microemulsifying drug delivery system (SMEDDS) of tacrolimus.Self-microemulsifiyng suppository formulation of β-artemether.In vitro and in vivo evaluation of self-microemulsifying drug delivery system of buparvaquone.Development and characterization of a lovastatin-loaded self-microemulsifying drug delivery system.Chemical drug stability in lipids, modified lipids, and polyethylene oxide-containing formulations.Development of self-microemulsifying drug delivery system for oral bioavailability enhancement of berberine hydrochloride.Solid self-microemulsifying drug delivery system of ritonavir.Preparation, characterization and in vitro intestinal absorption of a dry emulsion formulation containing atorvastatin calcium.High-throughput formulation screening system for self-microemulsifying drug delivery.Preparation and evaluation of Vinpocetine self-emulsifying pH gradient release pellets.In vitro and in vivo evaluations of the performance of an indirubin derivative, formulated in four different self-emulsifying drug delivery systemsDevelopment of Self-Emulsifying Drug Delivery Systems (SEDDS) for Oral Bioavailability Enhancement of Poorly Soluble Drugs
P2860
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P2860
Bioavailability of seocalcitol II: development and characterisation of self-microemulsifying drug delivery systems (SMEDDS) for oral administration containing medium and long chain triglycerides.
description
2006 nî lūn-bûn
@nan
2006 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Bioavailability of seocalcitol ...... and long chain triglycerides.
@ast
Bioavailability of seocalcitol ...... and long chain triglycerides.
@en
Bioavailability of seocalcitol ...... lsifying drug delivery systems
@nl
type
label
Bioavailability of seocalcitol ...... and long chain triglycerides.
@ast
Bioavailability of seocalcitol ...... and long chain triglycerides.
@en
Bioavailability of seocalcitol ...... lsifying drug delivery systems
@nl
prefLabel
Bioavailability of seocalcitol ...... and long chain triglycerides.
@ast
Bioavailability of seocalcitol ...... and long chain triglycerides.
@en
Bioavailability of seocalcitol ...... lsifying drug delivery systems
@nl
P2093
P1476
Bioavailability of seocalcitol ...... and long chain triglycerides.
@en
P2093
Gitte Pommergaard Pedersen
Jeanet Løgsted Nielsen
Mette Grove
P304
P356
10.1016/J.EJPS.2006.02.005
P407
P577
2006-05-02T00:00:00Z