Polylactic acid microspheres containing quinidine base and quinidine sulphate prepared by the solvent evaporation technique. I. Methods and morphology.
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Structural analysis of microparticles by confocal laser scanning microscopyEffects of formulation factors on encapsulation efficiency and release behaviour in vitro of huperzine A-PLGA microspheres.Effects of formulation parameters on encapsulation efficiency and release behavior of thienorphine loaded PLGA microspheres.Chitosan microcapsules as controlled release systems for insulin.Polylactic acid microspheres containing quinidine base and quinidine sulphate prepared by the solvent evaporation method. III. Morphology of the microspheres during dissolution studies.Simplex lattice design for the optimization of the microencapsulation of a water soluble drug using poly(lactic acid) and poly(lactide co-glycolide) copolymer.Encapsulation of hydrocortisone and mesalazine in zein microparticles.Gastroretentive microparticles for drug delivery applications.Biodegradable poly(lactic acid) and poly(lactide-co-glycolide) microcapsules: problems associated with preparative techniques and release properties.Controlled drug delivery by biodegradable poly(ester) devices: different preparative approaches.Optimization of the preparation of loperamide-loaded poly (L-lactide) nanoparticles by high pressure emulsification-solvent evaporation.Prospects of pharmaceuticals and biopharmaceuticals loaded microparticles prepared by double emulsion technique for controlled delivery.Air-filled polymeric microcapsules from emulsions containing different organic phases.Microencapsulation using poly (L-lactic acid) II: Preparative variables affecting microcapsule properties.Encapsulating acetaminophen into poly(L-lactide) microcapsules by solvent-evaporation technique in an O/W emulsion.Reduction in the initial-burst release by surface crosslinking of PLGA microparticles containing hydrophilic or hydrophobic drugs.Biodegradable poly(D, L-lactide-co-glycolide) (PLGA) microspheres for sustained release of risperidone: Zero-order release formulation.Some basic parameters of microspheres fabricated from a branched oligoester by a rapid procedure.In vitro degradation and dissolution behaviours of microspheres prepared by three low molecular weight polyesters.Functionality of protective colloids affecting the formation, size uniformity and morphology of drug-free polylactic acid microspheres.In Vitro-In Vivo Relationship of Amorphous Insoluble API (Progesterone) in PLGA Microspheres.Production of haloperidol-loaded PLGA nanoparticles for extended controlled drug release of haloperidol.Caffeic Acid Phenethyl Ester Loaded PLGA Nanoparticles: Effect of Various Process Parameters on Reaction Yield, Encapsulation Efficiency, and Particle Size
P2860
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P2860
Polylactic acid microspheres containing quinidine base and quinidine sulphate prepared by the solvent evaporation technique. I. Methods and morphology.
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年学术文章
@wuu
1987年学术文章
@zh
1987年学术文章
@zh-cn
1987年学术文章
@zh-hans
1987年学术文章
@zh-my
1987年学术文章
@zh-sg
1987年學術文章
@yue
1987年學術文章
@zh-hant
name
Polylactic acid microspheres c ...... ue. I. Methods and morphology.
@en
Polylactic acid microspheres c ...... ue. I. Methods and morphology.
@nl
type
label
Polylactic acid microspheres c ...... ue. I. Methods and morphology.
@en
Polylactic acid microspheres c ...... ue. I. Methods and morphology.
@nl
prefLabel
Polylactic acid microspheres c ...... ue. I. Methods and morphology.
@en
Polylactic acid microspheres c ...... ue. I. Methods and morphology.
@nl
P2860
P1476
Polylactic acid microspheres c ...... ue. I. Methods and morphology.
@en
P2093
J W McGinity
R Bodmeier
P2860
P304
P356
10.3109/02652048709021820
P577
1987-10-01T00:00:00Z