The use of solid self-emulsifying systems in the delivery of diclofenac.
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SHSST cyclodextrin complex prevents the fibrosis effect on CCl₄-induced cirrhotic cardiomyopathy in rats through TGF-β pathway inhibition effects.Preparation and evaluation of SEDDS and SMEDDS containing carvedilol.Preparation and pharmacokinetics evaluation of oral self-emulsifying system for poorly water-soluble drug Lornoxicam.Development and Evaluation of Novel Self-Nanoemulsifying Drug Delivery Systems Based on a Homolipid from Capra hircus and Its Admixtures with Melon Oil for the Delivery of IndomethacinLipid-based colloidal carriers for peptide and protein delivery--liposomes versus lipid nanoparticles.Extended release felodipine self-nanoemulsifying system.Sustained-release liquisolid compact tablets containing artemether-lumefantrine as alternate-day regimen for malaria treatment to improve patient complianceRole of excipients in successful development of self-emulsifying/microemulsifying drug delivery system (SEDDS/SMEDDS).Porous polystyrene beads as carriers for self-emulsifying system containing loratadine.Effect of formulation variables on preparation and evaluation of gelled self-emulsifying drug delivery system (SEDDS) of ketoprofen.Calcium Alginate-Neusilin US2 Nanocomposite Microbeads for Oral Sustained Drug Delivery of Poor Water Soluble Drug Aceclofenac Sodium.Formulation development and in vitro evaluation of solidified self-microemulsion in the form of tablet containing atorvastatin calcium.Enhanced ocular bioavailability of fluconazole from niosomal gels and microemulsions: formulation, optimization, and in vitro-in vivo evaluation.Formulation and evaluation of novel solid lipid microparticles as a sustained release system for the delivery of metformin hydrochloride.Pharmacodynamics of piroxicam from self-emulsifying lipospheres formulated with homolipids extracted from Capra hircus.Solid self-emulsifying drug delivery system (S-SEDDS) for improved dissolution rate of fenofibrate.Formulation in vitro and in vivo evaluation of SRMS-based heterolipid-templated homolipid delivery system for diclofenac sodium.QbD-based systematic development of novel optimized solid self-nanoemulsifying drug delivery systems (SNEDDS) of lovastatin with enhanced biopharmaceutical performance.
P2860
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P2860
The use of solid self-emulsifying systems in the delivery of diclofenac.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
@zh-hant
name
The use of solid self-emulsifying systems in the delivery of diclofenac.
@en
The use of solid self-emulsifying systems in the delivery of diclofenac.
@nl
type
label
The use of solid self-emulsifying systems in the delivery of diclofenac.
@en
The use of solid self-emulsifying systems in the delivery of diclofenac.
@nl
prefLabel
The use of solid self-emulsifying systems in the delivery of diclofenac.
@en
The use of solid self-emulsifying systems in the delivery of diclofenac.
@nl
P2093
P1476
The use of solid self-emulsifying systems in the delivery of diclofenac.
@en
P2093
P356
10.1016/S0378-5173(03)00315-6
P407
P577
2003-08-01T00:00:00Z