Transdermal Delivery of Glimepiride: A Novel Approach Using Nanomicelle-Embedded Microneedles

Glimepiride (GM) is a hydrophobic drug that dissolves slowly and yields inconsistent clinical responses after oral administration. Transdermal drug delivery (TDD) is an appropriate alternative to oral administration. Microneedles (MNs) offer a promising delivery system that penetrates the skin, whil...

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Main Authors: Sadia Pervez (Author), Fazli Nasir (Author), Talaya Hidayatullah (Author), Muzna Ali Khattak (Author), Fawaz Alasmari (Author), Syeda Rabqa Zainab (Author), Shazma Gohar (Author), Arbab Tahir (Author), Gul e Maryam (Author)
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Published: MDPI AG, 2023-07-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Sadia Pervez  |e author 
700 1 0 |a Fazli Nasir  |e author 
700 1 0 |a Talaya Hidayatullah  |e author 
700 1 0 |a Muzna Ali Khattak  |e author 
700 1 0 |a Fawaz Alasmari  |e author 
700 1 0 |a Syeda Rabqa Zainab  |e author 
700 1 0 |a Shazma Gohar  |e author 
700 1 0 |a Arbab Tahir  |e author 
700 1 0 |a Gul e Maryam  |e author 
245 0 0 |a Transdermal Delivery of Glimepiride: A Novel Approach Using Nanomicelle-Embedded Microneedles 
260 |b MDPI AG,   |c 2023-07-01T00:00:00Z. 
500 |a 10.3390/pharmaceutics15082019 
500 |a 1999-4923 
520 |a Glimepiride (GM) is a hydrophobic drug that dissolves slowly and yields inconsistent clinical responses after oral administration. Transdermal drug delivery (TDD) is an appropriate alternative to oral administration. Microneedles (MNs) offer a promising delivery system that penetrates the skin, while polymeric micelles can enhance the solubility; hence, the combination of both results in high drug bioavailability. This study aims to improve glimepiride's solubility, dissolution rate, and bioavailability by incorporating nanomicelles into MNs for TDD. The nanomicelles formulated with 10% Soluplus<sup>®</sup> (SP) and 40% GM had a mean particle size of 82.6 ± 0.54, PDI of 0.1 ± 0.01, −16.2 ± 0.18 zeta potential, and achieved a 250-fold increase in solubility. The fabricated pyramid shaped GM-dissolving MNs were thermally stable and had no formulation incompatibility, as confirmed by thermal and FTIR analysis. The in vitro dissolution profile revealed that the GM release from nanomicelles and nanomicelle-loaded DMN was concentration-independent following non-Fickian transport mechanism. Improved pharmacokinetic parameters were obtained with dose of 240 µg as compared to 1 mg of GM oral tablet, in healthy human volunteers. The observed C<sub>max</sub>, T<sub>max</sub> and MRT were 1.56 μg/mL ± 0.06, 4 h, and 40.04 h ± 3.37, respectively. The safety profile assessment indicated that microneedles are safe with no adverse effects on skin or health. This study provides an alternative delivery system for the administration of glimepiride, resulting in improved bioavailability, enhanced patient compliance, and reduced dosing frequency. 
546 |a EN 
690 |a glimepiride 
690 |a BCS class II drug 
690 |a transdermal drug delivery 
690 |a microneedles 
690 |a nanomicelles 
690 |a Soluplus<sup>®</sup> 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 15, Iss 8, p 2019 (2023) 
787 0 |n https://www.mdpi.com/1999-4923/15/8/2019 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/8d6da8d81b7042d3a74cff0f1893e988  |z Connect to this object online.