Literature DB >> 22555379

Development of a nanocrystalline Paclitaxel formulation for HIPEC treatment.

Lieselotte De Smet1, Pieter Colin, Wim Ceelen, Marc Bracke, Jan Van Bocxlaer, Jean Paul Remon, Chris Vervaet.   

Abstract

PURPOSE: To develop a nanocrystalline paclitaxel formulation with a high paclitaxel-to-stabilizer ratio which can be used for hyperthermic intraperitoneal chemotherapy (HIPEC).
METHODS: Paclitaxel (PTX) nanocrystals were prepared via wet milling using Pluronic F127(®) as stabilizer. The suitability of paclitaxel nanosuspensions for HIPEC treatment was evaluated by analyzing the cytotoxicity of both stabilizer and formulation, and by determining the maximum tolerated dose (MTD) and bioavailability. The effect on tumor growth was evaluated by magnetic resonance imaging (MRI) at day 7 and 14 after HIPEC treatment in rats with peritoneal carcinomatosis of ovarian origin.
RESULTS: Monodisperse nanosuspensions (±400 nm) were developed using Pluronic F127(®) as single additive. The cytotoxicity and MTD of this nanocrystalline formulation was similar compared to Taxol(®), while its bioavailability was higher. MRI data after HIPEC treatment with a PTX nanocrystalline suspension showed a significant reduction of tumor volume compared to the non-treated group. Although no significant differences on tumor volume were observed between Taxol(®) and the nanosuspension, the rats treated with the nanosuspension recovered faster following the HIPEC procedure.
CONCLUSION: Nanosuspensions with a high paclitaxel-to-stabilizer ratio are of interest for the treatment of peritoneal carcinomatosis of ovarian origin via HIPEC.

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Year:  2012        PMID: 22555379     DOI: 10.1007/s11095-012-0765-x

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  22 in total

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Review 3.  Comprehensive management of peritoneal surface malignancy using cytoreductive surgery and perioperative intraperitoneal chemotherapy: the Washington Cancer Institute approach.

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4.  Nanosuspensions of poorly soluble drugs: preparation and development by wet milling.

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5.  Nanosuspension for improving the bioavailability of a poorly soluble drug and screening of stabilizing agents to inhibit crystal growth.

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  11 in total

1.  A model based analysis of IPEC dosing of paclitaxel in rats.

Authors:  Pieter Colin; Lieselotte De Smet; Chris Vervaet; Jean-Paul Remon; Wim Ceelen; Jan Van Bocxlaer; Koen Boussery; An Vermeulen
Journal:  Pharm Res       Date:  2014-05-22       Impact factor: 4.200

2.  Nanocrystals for the parenteral delivery of poorly water-soluble drugs.

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4.  Development and evaluation of transferrin-stabilized paclitaxel nanocrystal formulation.

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5.  Optimal drug delivery for intraperitoneal paclitaxel (PTX) in murine model.

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6.  Pretreatment with VEGF(R)-inhibitors reduces interstitial fluid pressure, increases intraperitoneal chemotherapy drug penetration, and impedes tumor growth in a mouse colorectal carcinomatosis model.

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7.  Preclinical evaluation of local prolonged release of paclitaxel from gelatin microspheres for the prevention of recurrence of peritoneal carcinomatosis in advanced ovarian cancer.

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Review 8.  Optimization of drug delivery systems for intraperitoneal therapy to extend the residence time of the chemotherapeutic agent.

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Review 10.  Parenteral nanosuspensions: a brief review from solubility enhancement to more novel and specific applications.

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