Pre-Clinical Investigation of Liquid Paclitaxel for Local Drug Delivery: A Pilot Study.

liquid paclitaxel local drug delivery perfusion catheter peripheral arterial disease pre-clinical modeling

Journal

Pharmaceuticals (Basel, Switzerland)
ISSN: 1424-8247
Titre abrégé: Pharmaceuticals (Basel)
Pays: Switzerland
ID NLM: 101238453

Informations de publication

Date de publication:
28 Nov 2020
Historique:
received: 25 09 2020
revised: 17 11 2020
accepted: 24 11 2020
entrez: 2 12 2020
pubmed: 3 12 2020
medline: 3 12 2020
Statut: epublish

Résumé

The purpose of this pilot study was to investigate the feasibility of a perfusion catheter to deliver liquid paclitaxel into arterial segments. A clinically relevant rabbit ilio-femoral injury model was utilized to determine the impact of liquid paclitaxel delivered locally into the vessel wall using a perfusion catheter at 1 h to 14 days. Treatment by two clinically available forms of liquid paclitaxel, a solvent-based (sb) versus an albumin-bound (nab), along with a control (uncoated balloons), were investigated. Pharmacokinetic results demonstrated an increase in the retention of the sb-paclitaxel versus the nab-paclitaxel at 1 h; however, no other differences were observed at days one, three, and seven. Histological findings at 14 days showed significantly less neointimal area in the sb-paclitaxel treated arteries as compared with the nab-paclitaxel and the uncoated balloon-treated arteries. Additionally, percent area stenosis was significantly less in the sb-paclitaxel group. These results support the concept of local liquid delivery of paclitaxel into the arterial segments.

Identifiants

pubmed: 33260517
pii: ph13120434
doi: 10.3390/ph13120434
pmc: PMC7760562
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : NHLBI NIH HHS
ID : R15 HL127596
Pays : United States
Organisme : NIBIB NIH HHS
ID : R01 EB028798
Pays : United States
Organisme : American Heart Association
ID : 15SDG25880000
Organisme : NIH HHS
ID : 1R01EB028798
Pays : United States
Organisme : NIH HHS
ID : 1R15HL127596
Pays : United States

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Auteurs

Claire V Cawthon (CV)

Department of Mechanical Engineering, University of South Alabama, Mobile, AL 36688, USA.

Kathryn Cooper (K)

Department of Mechanical Engineering, University of South Alabama, Mobile, AL 36688, USA.

Clifton Huett (C)

Department of Mechanical Engineering, University of South Alabama, Mobile, AL 36688, USA.

Alyssa Lloret (A)

Department of Engineering, Wake Forest University, Winston-Salem, NC 27101, USA.

Estefanny Villar-Matamoros (E)

Department of Engineering, Wake Forest University, Winston-Salem, NC 27101, USA.

Lauren Stokes (L)

Department of Engineering, Wake Forest University, Winston-Salem, NC 27101, USA.

Uwe Christians (U)

iC42 Clinical Research and Development, University of Colorado, Aurora, CO 80045, USA.

Michele Schuler (M)

Department of Comparative Medicine, University of South Alabama, Mobile, AL 36688, USA.

Saami K Yazdani (SK)

Department of Engineering, Wake Forest University, Winston-Salem, NC 27101, USA.

Classifications MeSH