Development of solid self-emulsifying drug delivery systems: preparation techniques and dosage forms.
about
Controlled release systems containing solid dispersions: strategies and mechanismsNovel gastroretentive sustained-release tablet of tacrolimus based on self-microemulsifying mixture: in vitro evaluation and in vivo bioavailability test.Solid-nanoemulsion preconcentrate for oral delivery of paclitaxel: formulation design, biodistribution, and γ scintigraphy imaging.Development and evaluation of a solid self-nanoemulsifying drug delivery system for loratadin by extrusion-spheronizationDevelopment and characterization of nanoemulsion as carrier for the enhancement of bioavailability of artemether.Single and dual drug release patterns from shellac wax-lutrol matrix tablets fabricated with fusion and molding techniques.Preparation and in vivo evaluation of a dutasteride-loaded solid-supersaturatable self-microemulsifying drug delivery system.Design of a gelatin microparticle-containing self-microemulsifying formulation for enhanced oral bioavailability of dutasteride.Comparative study on solid self-nanoemulsifying drug delivery and solid dispersion system for enhanced solubility and bioavailability of ezetimibe.Design, optimization and evaluation of glipizide solid self-nanoemulsifying drug delivery for enhanced solubility and dissolution.Microemulsions as drug delivery systems to improve the solubility and the bioavailability of poorly water-soluble drugs.Oral formulation strategies to improve solubility of poorly water-soluble drugs.Has nanotechnology led to improved therapeutic outcomes?Transforming lipid-based oral drug delivery systems into solid dosage forms: an overview of solid carriers, physicochemical properties, and biopharmaceutical performance.Self-microemulsifying drug delivery system (SMEDDS)--challenges and road ahead.Strategies for oral delivery and mitochondrial targeting of CoQ10.Oral bioavailability: issues and solutions via nanoformulations.Novel Nanostructured Solid Materials for Modulating Oral Drug Delivery from Solid-State Lipid-Based Drug Delivery Systems.From nanoemulsions to self-nanoemulsions, with recent advances in self-nanoemulsifying drug delivery systems (SNEDDS).Evaluation of Spray BIO-Max DIM-P in Dogs for Oral Bioavailability and in Nu/nu Mice Bearing Orthotopic/Metastatic Lung Tumor Models for Anticancer Activity.Controversies with self-emulsifying drug delivery system from pharmacokinetic point of view.Comparison of cytotoxicity in vitro and irritation in vivo for aqueous and oily solutions of surfactants.Design, characterization and in vitro evaluation of SMEDDS containing an anticancer peptide, linear LyP-1.Preformulation studies on solid self-emulsifying systems in powder form containing magnesium aluminometasilicate as porous carrier.Novel Solid Self-Nanoemulsifying Drug Delivery System (S-SNEDDS) for Oral Delivery of Olmesartan Medoxomil: Design, Formulation, Pharmacokinetic and Bioavailability Evaluation.The utility of self-emulsifying oil formulation to improve the poor solubility of the anti HIV drug CSIC.A comparison between use of spray and freeze drying techniques for preparation of solid self-microemulsifying formulation of valsartan and in vitro and in vivo evaluation.Self micro-emulsifying drug delivery system of tacrolimus: Formulation, in vitro evaluation and stability studiesDevelopment, optimization, and characterization of solid self-nanoemulsifying drug delivery systems of valsartan using porous carriers.Development of Solid SEDDS, V: Compaction and Drug Release Properties of Tablets Prepared by Adsorbing Lipid-Based Formulations onto Neusilin® US2.Folate-conjugated PEG on single walled carbon nanotubes for targeting delivery of Doxorubicin to cancer cells.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.Solidified self-nanoemulsifying formulation for oral delivery of combinatorial therapeutic regimen: part I. Formulation development, statistical optimization, and in vitro characterization.Supersaturable solid self-microemulsifying drug delivery system: precipitation inhibition and bioavailability enhancement.Proliposome powders for enhanced intestinal absorption and bioavailability of raloxifene hydrochloride: effect of surface charge.Effects of crystalline state and self-nanoemulsifying drug delivery system (SNEDDS) on oral bioavailability of the novel anti-HIV compound 6-benzyl-1-benzyloxymethyl-5-iodouracil in rats.Design of a novel type IV lipid-based delivery system for improved delivery of drugs with low partition coefficient.QbD-based systematic development of novel optimized solid self-nanoemulsifying drug delivery systems (SNEDDS) of lovastatin with enhanced biopharmaceutical performance.A solid self-nanoemulsifying system of the BCS class IIb drug dabigatran etexilate to improve oral bioavailability.
P2860
Q24301733-D0A11ECC-44CF-4B6B-B1D0-297424EDA818Q33566190-A088D6B5-7A2A-44C7-A520-D7CFDA2BBD9EQ33999835-F74B50C6-72CF-48D3-A352-8BAEF7B645CAQ35089750-D2CE8C29-7E0A-4A16-AB20-6C23FABF5D47Q35123659-D29E3782-FB8C-4676-A909-458DB41F796BQ35166232-69212ADD-70D5-4011-B7C3-3F06111CD1C0Q35723500-AA6D8C05-90EF-4FF2-8D61-996DD49307EAQ35794494-269E3E73-EE2D-4A35-80E4-E328861DD443Q36137372-702C30FD-2285-41B8-96B5-CF45BC956DF3Q36162058-B9609C2E-F1C7-49CF-9C02-B9A19C6B22D5Q37702234-BEF41950-8615-4A99-B516-BAB691C66A98Q37910262-2DD45F82-5059-4C8A-BD43-33334B15EE29Q37970730-C42C6903-4CE1-4DEA-BEE9-FED29B283264Q38115195-54D571F6-6467-4A07-9584-E0E75A9EDC87Q38199539-E5B675B3-4FFB-42AC-8D4B-FE8985A5F098Q38301993-073F618A-7118-4B65-937C-EE3F580C08BAQ38349734-2DB20B45-5AD8-497C-8F13-DFDC3C5717DBQ38583850-3595EFB3-C828-4560-8108-F47F47FD34CAQ38916539-43D35360-BDEA-4602-B99A-09694408DF23Q38921461-7829B501-13D7-47C5-A8C3-F849FB06CCA0Q38967883-2B47DFC9-1B04-4D8E-88F8-C0D2F00BF1B0Q38975634-C09FB8EE-6412-425F-9060-0CF35EA2CEF0Q39151249-8B3D7284-C523-4168-B406-F3B438174837Q41110566-DEFE979E-6ECC-4C80-8624-AA8B67B94D42Q41201676-60C48B55-31E5-451B-BB19-B886CECAEA19Q41832847-4F47853A-81A5-49AE-B320-9348AA6D3762Q41845360-08CA0BB7-D240-4ED7-B830-F8E9479FF3F8Q41939998-C9AE33D4-CC1B-408C-BD6D-DF895685737EQ41988146-0CCA4827-1FEB-421F-8196-EE310964C1FDQ42216132-69971BF7-E9BA-4223-BA6E-ACD840E3D7F4Q42820624-84A1D3C6-F727-40B4-94AF-B92F812F00BDQ43179848-30883D59-7CE6-46F0-9FB3-8A344BB7784EQ44367296-5B22DEAC-605A-4857-9280-E36416886D17Q44575462-EF76AAEE-AD98-4904-904F-8CA4EAECC967Q47141833-1B51E128-E909-4AA7-BCD6-2617BC328EEBQ47970921-BAE0245B-C142-4FBA-A5E8-91C8176724C9Q48608254-261023CB-5458-420F-8FB4-4E8571ED67F0Q50998576-2D85B93D-18B0-4C53-9894-B55A2B96DB19Q51099269-E812C970-B1AD-4C4D-8A3F-ADD6F63556F8Q51255753-73111F60-A92C-489D-8C0F-F72A3DA9D27C
P2860
Development of solid self-emulsifying drug delivery systems: preparation techniques and dosage forms.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 03 June 2008
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Development of solid self-emul ...... n techniques and dosage forms.
@en
Development of solid self-emul ...... n techniques and dosage forms.
@nl
type
label
Development of solid self-emul ...... n techniques and dosage forms.
@en
Development of solid self-emul ...... n techniques and dosage forms.
@nl
prefLabel
Development of solid self-emul ...... n techniques and dosage forms.
@en
Development of solid self-emul ...... n techniques and dosage forms.
@nl
P2093
P1433
P1476
Development of solid self-emul ...... n techniques and dosage forms.
@en
P2093
Cai-Hong Xu
Gang Cheng
Jian-Chun Gu
P304
P356
10.1016/J.DRUDIS.2008.04.006
P577
2008-06-03T00:00:00Z