Source: Journal of Pharmaceutical Sciences. Mar2015, Vol. 104 Issue 3, p1099-1107. 9p. 3 Color Photographs, 3 Black and White Photographs, 1 Chart, 3 Graphs.

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Academic Journal

Binary Graft Modification of Polypropylene for Anti-Inflammatory Drug-Device Combo Products.

Authors : Melendez-Ortiz, Hector Ivan^1,2; Díaz-Rodríguez, Patricia²; Alvarez-Lorenzo, Carmen²

Subjects: *POLYPROPYLENE; *ANTI-inflammatory agents; *DRUG delivery devices

Source: Journal of Pharmaceutical Sciences. Apr2014, Vol. 103 Issue 4, p1269-1277. 9p.

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Pharmaceutical aspects of drug eluting stents

Authors : E. Deconinck; Jurgen Sohier; I. De Scheerder

Subjects: Drug; medicine.medical_specialty; Research areas

Source: Journal of pharmaceutical sciences. 97(12)

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Academic Journal

In vivo evaluation of 5-fluorouracil-containing self-expandable nitinol stent in rabbits: Efficiency in long-term local drug delivery.

Authors : Guo SR; School of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, China. ; Wang ZM

Subjects: Alloys*/Alloys*/Alloys*/chemistry ; Drug-Eluting Stents*; Antimetabolites, Antineoplastic/Antimetabolites, Antineoplastic/Antimetabolites, Antineoplastic/*administration & dosage

Source: Journal of pharmaceutical sciences [J Pharm Sci] 2010 Jul; Vol. 99 (7), pp. 3009-18.Publisher: Elsevier Country of Publication: United States NLM ID: 2985195R Publication Model: Print Cited Medium: Internet ISSN: 1520-6017

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Intravascular bioresorbable polymeric stents: a potential alternative to current drug eluting metal stents.

Authors : Sharkawi T; Artificial Biopolymer Research Center, UMR CNRS 5473, Faculty of Pharmacy, University of Montpellier 1, 15 av Charles Flahaut, 34093 Montpellier, Cedex, France. ; Cornhill F

Subjects: Absorbable Implants* ; Drug-Eluting Stents*; Lactic Acid/Lactic Acid/Lactic Acid/*administration & dosage

Source: Journal of pharmaceutical sciences [J Pharm Sci] 2007 Nov; Vol. 96 (11), pp. 2829-37.Publisher: Elsevier Country of Publication: United States NLM ID: 2985195R Publication Model: Print Cited Medium: Print ISSN: 0022-3549 (Print)

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Composite fiber structures with antiproliferative agents exhibit advantageous drug delivery and cell growth inhibition in vitro.

Authors : Kraitzer A; Faculty of Engineering, Department of Biomedical Engineering, Tel-Aviv University, Tel-Aviv 69978, Israel.; Kloog Y

Subjects: Drug Delivery Systems*; Antineoplastic Agents/Antineoplastic Agents/Antineoplastic Agents/*chemistry ; Antineoplastic Agents/Antineoplastic Agents/Antineoplastic Agents/*pharmacology

Source: Journal of pharmaceutical sciences [J Pharm Sci] 2011 Jan; Vol. 100 (1), pp. 133-49. Date of Electronic Publication: 2010 Jul 08.Publisher: Elsevier Country of Publication: United States NLM ID: 2985195R Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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In vitro evaluation of cenderitide-eluting stent I -an antirestenosis and proendothelization approach

Authors : Yingying Huang; Subbu S. Venkatraman; Yin Chiang Freddy Boey

Subjects: peptide delivery; Polyesters; Myocytes, Smooth Muscle

Source: Journal of pharmaceutical sciences. 103(11)

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نتائج البحث

فلترة النتائج

Pharmaceutical aspects of drug eluting stents.

Impact of artificial plaque composition on drug transport.

In Vitro Evaluation of Cenderitide-Eluting Stent I -An Antirestenosis and Proendothelization Approach.

Three-Dimensional Printing of Drug-Eluting Implants: Preparation of an Antimicrobial Polylactide Feedstock Material.

Binary Graft Modification of Polypropylene for Anti-Inflammatory Drug-Device Combo Products.

Pharmaceutical aspects of drug eluting stents

In vivo evaluation of 5-fluorouracil-containing self-expandable nitinol stent in rabbits: Efficiency in long-term local drug delivery.

Intravascular bioresorbable polymeric stents: a potential alternative to current drug eluting metal stents.

Composite fiber structures with antiproliferative agents exhibit advantageous drug delivery and cell growth inhibition in vitro.

In vitro evaluation of cenderitide-eluting stent I -an antirestenosis and proendothelization approach

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