Nanoencapsulation of Fenretinide in Glucosamine Butyrate - GelatinMatrices as a Mean to Improve its Oral Bioavailability

Fenretinide (4-HPR) is the most promising retinoid derivative with anticancer activity and low toxicity profile. Despite its excellent tolerability, the formulations of 4-HPR that have been clinically evaluated until now have not provided drug plasma concentrations suitable to elicit a therapeutic response. Therefore innovative formulations able to improve the drug bioavailability would be of considerable interest. In this work we describe the preparation and functional evaluation of novel nanocapsules designed to enhance fenretinide bioavailability by oral route through the use of glucosamine butyrate as bioavailability enhancer and gelatin as a matrix forming agent. The anti-tumour activity of the nanocapsules has been tested in in vitro and in vivo models either in feeding and fasting conditions. Our data indicated that after oral administration the nanocapsules provide 4-HPR plasma concentrations in the range compatible with the antitumor activity as assessed in vitro expecially in fasting conditions. Moreover these novel nanocapsules have proved to be effective in tumor xenografts after oral administration.

[1]  A. Tesei,et al.  Anti-tumor activity of fenretinide complexed with human serum albumin in lung cancer xenograft mouse model , 2014, Oncotarget.

[2]  M. Falconi,et al.  Novel PLA microspheres with hydrophilic and bioadhesive surfaces for the controlled delivery of fenretinide , 2014, Journal of microencapsulation.

[3]  J. Kanwar,et al.  Natural antioxidant biomolecules promises future nanomedicine based therapy for cataract. , 2013, Colloids and surfaces. B, Biointerfaces.

[4]  S. Guterres,et al.  Poly(ϵ-caprolactone) microcapsules and nanocapsules in drug delivery , 2013, Expert opinion on drug delivery.

[5]  M. Falconi,et al.  Novel micelles based on amphiphilic branched PEG as carriers for fenretinide. , 2012, Nanomedicine : nanotechnology, biology, and medicine.

[6]  A. Naranjo,et al.  Phase II Study of Oral Capsular 4-Hydroxyphenylretinamide (4-HPR/Fenretinide) in Pediatric Patients with Refractory or Recurrent Neuroblastoma: A Report from the Children's Oncology Group , 2011, Clinical Cancer Research.

[7]  P. Kovacs,et al.  Influence of food on the pharmacokinetics of oral alitretinoin (9‐cis retinoic acid) , 2011, Clinical and experimental dermatology.

[8]  S. Mitragotri,et al.  Safe and Effective Permeation Enhancers for Oral Drug Delivery , 2008, Pharmaceutical Research.

[9]  S. Mitragotri,et al.  Mechanistic Analysis of Chemical Permeation Enhancers for Oral Drug Delivery , 2008, Pharmaceutical Research.

[10]  W. Shaw,et al.  Improved Oral Delivery of N-(4-Hydroxyphenyl)Retinamide with a Novel LYM-X-SORB Organized Lipid Complex , 2007, Clinical Cancer Research.

[11]  David J Brayden,et al.  Promoting absorption of drugs in humans using medium-chain fatty acid-based solid dosage forms: GIPET™ , 2006, Expert opinion on drug delivery.

[12]  S. Dixon,et al.  N-Butyryl Glucosamine Increases Matrix Gene Expression by Chondrocytes , 2004, Journal of Pharmacology and Experimental Therapeutics.

[13]  B. Maurer,et al.  Liquid chromatography method for quantifying N-(4-hydroxyphenyl)retinamide and N-(4-methoxyphenyl)retinamide in tissues. , 2004, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[14]  L. Boni,et al.  Phase I trial and pharmacokinetics of fenretinide in children with neuroblastoma. , 2003, Clinical cancer research : an official journal of the American Association for Cancer Research.

[15]  P. Couvreur,et al.  Nanoparticles in cancer therapy and diagnosis. , 2002, Advanced drug delivery reviews.

[16]  R. Nayak,et al.  Effects of Meals and Meal Composition on the Bioavailability of Fenretinide , 1992, Journal of clinical pharmacology.

[17]  P. McNamara,et al.  Food Increases the Bioavailability of Acitretin , 1988, Journal of clinical pharmacology.

[18]  W. Colburn,et al.  Food Increases the Bioavailability of Isotretinoin , 1983, Journal of clinical pharmacology.