Enhancement of bioavailability through transdermal drug delivery of paliperidone palmitate-loaded nanostructured lipid carriers

Aim: The work describes enhanced bioavailability of paliperidone palmitate through transdermal delivery using nanostructured lipid carriers (NLC). Materials & methods: NLCs were formulated by nanoprecipitation method followed by incorporation in transdermal patch and physicochemical characterization. Results: NLCs showed high percentage entrapment efficiency of 83.44 ± 0.8%, drug loading of 24.75 ± 1.10% (w/w), particle size of 173.8 ± 3.25 nm, polydispersity index of 0.143 ± 0.05 and zeta potential of -15.9 ± 0.75 mV. In vitro and ex vivo studies indicated zero-order controlled drug release from NLCs and transdermal patch up to 48 h. Pharmacokinetic studies indicated 1.76-fold enhanced bioavailability by transdermal route as compared with oral drug delivery. Conclusion: From the results, it was concluded that drug-loaded NLCs-transdermal patch is promising drug delivery system for poorly bioavailable drugs.

Medienart:

E-Artikel

Erscheinungsjahr:

2021

Erschienen:

2021

Enthalten in:

Zur Gesamtaufnahme - volume:12

Enthalten in:

Therapeutic delivery - 12(2021), 8 vom: 04. Aug., Seite 583-596

Sprache:

Englisch

Beteiligte Personen:

Raval, Shilpa [VerfasserIn]
Jani, Parva [VerfasserIn]
Patil, Pravin [VerfasserIn]
Thakkar, Parth [VerfasserIn]
Sawant, Krutika [VerfasserIn]

Links:

Volltext

Themen:

Bioavailability
Drug Carriers
Journal Article
Lipids
Nanostructured lipid carriers
Paliperidone Palmitate
Paliperidone palmitate
R8P8USM8FR
Research Support, Non-U.S. Gov't
Schizophrenia
Transdermal

Anmerkungen:

Date Completed 02.08.2021

Date Revised 02.08.2021

published: Print-Electronic

Citation Status MEDLINE

doi:

10.4155/tde-2021-0036

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM328317055