3D printed, controlled release, tritherapeutic tablet matrix for advanced anti-HIV-1 drug delivery.
Alkynes
Animals
Anti-HIV Agents
/ administration & dosage
Benzoxazines
/ administration & dosage
Cyclopropanes
Delayed-Action Preparations
/ administration & dosage
Drug Liberation
/ drug effects
Emtricitabine
/ administration & dosage
HIV Infections
/ economics
HIV-1
/ drug effects
Humans
Printing, Three-Dimensional
Swine
Tablets
/ administration & dosage
Tenofovir
/ administration & dosage
3D printing
Anti-HIV-1 drugs
Efavirenz
Emtricitabine
Fixed dose combination
Tenofovir disoproxil fumarate
Journal
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V
ISSN: 1873-3441
Titre abrégé: Eur J Pharm Biopharm
Pays: Netherlands
ID NLM: 9109778
Informations de publication
Date de publication:
May 2019
May 2019
Historique:
received:
18
01
2018
revised:
09
04
2018
accepted:
11
04
2018
pubmed:
16
4
2018
medline:
15
8
2019
entrez:
16
4
2018
Statut:
ppublish
Résumé
A 3D-Bioplotter® was employed to 3D print (3DP) a humic acid-polyquaternium 10 (HA-PQ10) controlled release fixed dose combination (FDC) tablet comprising of the anti-HIV-1 drugs, efavirenz (EFV), tenofovir disoproxil fumarate (TDF) and emtricitabine (FTC). Chemical interactions, surface morphology and mechanical strength of the FDC were ascertained. In vitro drug release studies were conducted in biorelevant media followed by in vivo study in the large white pigs, in comparison with a market formulation, Atripla®. In vitro-in vivo correlation of results was undertaken. EFV, TDF and FTC were successfully entrapped in the 24-layered rectangular prism-shaped 3DP FDC with a loading of ∼12.5 mg/6.3 mg/4 mg of EFV/TDF/FTC respectively per printed layer. Hydrogen bonding between the EFV/TDF/FTC and HA-PQ10 was detected which was indicative of possible drug solubility enhancement. The overall surface of the tablet exhibited a fibrilla structure and the 90° inner pattern was determined to be optimal for 3DP of the FDC. In vitro and in vivo drug release profiles from the 3DP FDC demonstrated that intestinal-targeted and controlled drug release was achieved. A 3DP FDC was successfully manufactured with the aid of a 3D-Bioplotter in a single step process. The versatile HA-PQ10 entrapped all drugs and achieved an enhanced relative bioavailability of EFV, TDF, and FTC compared to the market formulation for potentially enhanced HIV treatment.
Identifiants
pubmed: 29655904
pii: S0939-6411(18)30049-3
doi: 10.1016/j.ejpb.2018.04.007
pii:
doi:
Substances chimiques
Alkynes
0
Anti-HIV Agents
0
Benzoxazines
0
Cyclopropanes
0
Delayed-Action Preparations
0
Tablets
0
Tenofovir
99YXE507IL
Emtricitabine
G70B4ETF4S
efavirenz
JE6H2O27P8
Types de publication
Journal Article
Langues
eng
Pagination
99-110Informations de copyright
Copyright © 2018 Elsevier B.V. All rights reserved.