Literature DB >> 29366416

Finasteride Topical Delivery Systems for Androgenetic Alopecia.

Muhammad Z U Khan1, Shujaat A Khan1, Muhammad Ubaid1, Aamna Shah1, Rozina Kousar1, Ghulam Murtaza1.   

Abstract

Androgenetic alopecia, generally recognized as male pattern baldness, is a gradually developing medical and physiological change, which is manifested by continuous hair-loss from scalp. Finasteride (4-aza-3-oxosteroid) is a potent anti-baldness compound that selectively and competitively inhibits the 5α-reductase isoenzymes. Prolonged oral use of finasteride leads to the emergence of sexual disorders including decrease in libido, gynecomastia, erectile dysfunction, ejaculation disorder, orgasm disorders and mood disturbances. Since, hair follicles widely home in 5α-reductase, topical formulations of finasteride in comparison to its oral formulations are expected to potentially reduce its systemic adverse effects. The analysis of literature has revealed some delivery systems developed for the enhanced and localized penetration of finasteride into the skin. These finasteride delivery systems include polymersomes, vesicular nanocarriers, vesicular ethosomal carriers, liposomes and niosomes, liquid crystalline nanoparticles, topical solutions and gels. The aim of this review article is to briefly amass all literature on topical delivery of finasteride to elaborate best dosage form, i.e. formulation having maximum permeation rate. This study will serve as a future perspective regarding topical delivery of finasteride. The literature analysis has exhibited that most of the previous investigators have used propylene glycol in their finasteride-loaded topical formulations, while poloxamer P407, monoolein, transcutol P and choline was used in few formulations. Moreover, among all drug delivery systems, finasteride liposomal gel system consisting of 2% methyl cellulose and gel system containing poloxamer P407 exhibited the highest flux with a value of 28.4 ± 1.3 µg/cm2h and 23.1 ± 1.4 µg/cm2h, respectively. Several topical drug delivery techniques such as topical microneedles, aerosol foams, nanoemulsions, microsponges, and emulsifier free formulations, fullerenes, ointments, pastes, creams, gel and lotions are still to be worthy regarding finasteride topical delivery in future. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.

Entities:  

Keywords:  5α-reductase isoenzymes; Androgenetic alopecia; Erectile dysfunction; Finasteride; Flux; Propylenezzm321990glycol; Topical formulation.

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Year:  2018        PMID: 29366416     DOI: 10.2174/1567201815666180124112905

Source DB:  PubMed          Journal:  Curr Drug Deliv        ISSN: 1567-2018            Impact factor:   2.565


  4 in total

1.  Protective effects of finasteride against testosterone-induced calcium oxalate crystallization and crystal-cell adhesion.

Authors:  Kanyarat Sueksakit; Visith Thongboonkerd
Journal:  J Biol Inorg Chem       Date:  2019-07-24       Impact factor: 3.358

2.  Drug Delivery System Based On Minoxidil Nanoparticles Promotes Hair Growth In C57BL/6 Mice.

Authors:  Noriaki Nagai; Yoshie Iwai; Akane Sakamoto; Hiroko Otake; Yoshihiro Oaku; Akinari Abe; Tohru Nagahama
Journal:  Int J Nanomedicine       Date:  2019-10-01

3.  Finasteride-loaded nano-lipidic carriers for follicular drug delivery: preformulation screening and Box-Behnken experimental design for optimization of variables.

Authors:  Shweta Ramkar; Preeti K Suresh
Journal:  Heliyon       Date:  2022-08-15

4.  Physicochemical Characterization of Finasteride Nanosystem for Enhanced Topical Delivery.

Authors:  Malik Muhammad Irfan; Shefaat Ullah Shah; Ikram Ullah Khan; Muhammad Usman Munir; Nauman Rahim Khan; Kifayat Ullah Shah; Saif Ur Rehman; Muhammad Sohaib; Hafiz Muhammad Basit; Saima Mahmood
Journal:  Int J Nanomedicine       Date:  2021-02-16
  4 in total

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