Paclitaxel-Loaded Gelatin Nanoparticles for Intravesical Bladder Cancer Therapy

• Published in: Clinical cancer research Vol. 10; no. 22; pp. 7677 - 7684
• Main Authors: Lu, Ze, Yeh, Teng-Kuang, Tsai, Max, Au, Jessie L.-S., Wientjes, M. Guill
• Format: Journal Article
• Language: English
• Published: Philadelphia, PA American Association for Cancer Research 15.11.2004
• Subjects: Animals; Antineoplastic agents; Antineoplastic Agents, Phytogenic - administration & dosage; Antineoplastic Agents, Phytogenic - pharmacokinetics; Biological and medical sciences; Chromatography, High Pressure Liquid; Dogs; Dose-Response Relationship, Drug; Drug Delivery Systems; Gelatin - chemistry; Gelatin - pharmacokinetics; Male; Medical sciences; Micelles; Nanostructures - chemistry; Nanotechnology; Nephrology. Urinary tract diseases; Paclitaxel - administration & dosage; Paclitaxel - pharmacokinetics; Pharmacology. Drug treatments; Polyethylene Glycols; Time Factors; Tumors of the urinary system; Urinary Bladder - metabolism; Urinary Bladder Neoplasms - drug therapy; Urinary system involvement in other diseases. Miscellaneous; Urinary tract. Prostate gland; X-Ray Diffraction; Antineoplastic agent; Load; Urinary system disease; Nanoparticle; Malignant tumor; Urinary tract disease; Bladder cancer; Treatment; Gelatin; Taxane derivatives; Paclitaxel; Bladder disease; Antimitotic
• DOI: 10.1158/1078-0432.CCR-04-1443
• ISSN: 1078-0432

Purpose: The present report describes the development of paclitaxel-loaded gelatin nanoparticles for use in intravesical therapy of superficial bladder cancer. The commercial formulation of paclitaxel contains Cremophor, which forms micelles and thereby entraps the drug and reduces its partition across the urothelium. Experimental Design: Paclitaxel-loaded gelatin nanoparticles were prepared using the desolvation method, and their physicochemical and biological properties were characterized. Results: The size of the particles ranged from 600 to 1,000 nm and increased with the molecular weight of the gelatin polymer. Under optimal conditions, the yield was >80%, and the drug loading was 0.7%. Wide-angle X-ray diffraction analysis showed that the entrapped paclitaxel was present in an amorphous state, which has higher water solubility compared with the crystalline state. Identical, rapid drug release from nanoparticles was observed in PBS and urine, with ∼90% released at 37°C after 2 hours. Treatment with a protease ( i.e ., Pronase) rapidly degraded the nanoparticles, with half-lives of 23.8 minutes, 0.6 minute, and 0.4 minute in the presence of 0.01, 0.05, and 0.25 mg/mL Pronase, respectively. The paclitaxel-loaded nanoparticles were active against human RT4 bladder transitional cancer cells; the IC 50 paclitaxel-equivalent concentrations were nearly identical to those of aqueous solutions of paclitaxel, i.e ., ∼30 nmol/L (equivalent to ∼25 ng/mL) for 2-hour treatments and ∼4 nmol/L for 96-hour treatments. In dogs given an intravesical dose of paclitaxel-loaded particles, the drug concentrations in the urothelium and lamina propria tissue layers, where Ta and T1 tumors would be located, were 7.4 ± 4.3 μg/g (mean ± SD; 3 dogs; 9 tissue sections), which were 2.6× the concentrations we reported for dogs treated with the Cremophor formulation. Conclusions: Paclitaxel-loaded gelatin nanoparticles represent a rapid release, biologically active paclitaxel formulation that can be used for intravesical bladder cancer therapy.