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The DOI matches its Crossref record; 44 of the 44 references it cites were found in a registry or an index; none of the 24 sources its claims cite is checked for support yet.

Formulation and Characterization of PLGA Minocycline Microneedles for Enhanced Skin Deposition and Antibacterial Activity in Acne Treatment

Open access
Abu Ershaid, Juhaina M., Abudoleh, Suha M., Lafi, Dima N., Dahshan, Nisreen A.·2025·Polymers

Abstract

Acne is a multifactorial skin condition characterized by an infection in the pilosebaceous units in the skin. Patients with acne suffer from comedones, papules, pustules and nodules or cysts in severe cases. These clinical features might cause disfigurmentation, depression, anxiety and significantly impact the quality of life of patients. Systemic and continuous exposure of antibiotics put patients at risk of developing systemic toxicity, bacterial resistance and gut dysbiosis. Microneedles offer an innovative approach of providing targeted topical delivery of minocycline while insuring efficient permeation through skin layers. Methods: minocycline microneedles were formulated using casting method and characterized for insertion ability, mechanical strength, drug content, antibacterial activities, deposition and dissolution behavior using ex vivo full-thickness rat skin. Results: Insertion tests confirmed effective skin penetration and mechanical integrity with only 9.5% height reduction. Drug content was 673.06 ± 5.34 µg/array. Dissolution occurred within 2 min in skin, indicating user-friendly wear time. Ex vivo Franz diffusion studies showed 26% of the drug deposited into the skin, significantly higher (p = 0.0068) than the 18.3% that permeated through it. Antibacterial testing revealed strong activity against S. aureus, S. epidermidis, and C. acnes, with MIC values < 0.146 µg/mL and MBC values ranging from 9.375–18.75 µg/mL. Conclusions: The result of this research demonstrate that minocycline microneedles effectively deliver minocycline into the skin highlighting their potential as a safer and more efficient alternative for acne therapy.

Overview

CoChat Summary

TL;DR

PLGA tipped microneedles loaded with minocycline were successfully fabricated and characterized for acne treatment. They showed mechanical integrity, rapid skin dissolution, higher skin deposition than permeation, and preserved antibacterial activity against acne-associated bacteria.

Key findings

  • Insertion and mechanical tests confirmed effective skin penetration and no mechanical failure; Parafilm® M first layer was penetrated at 100%, the second layer was reached (252 µm insertion depth), and height reduction after compression was 9.5 ± 5.6%.
  • Drug content was 673.06 ± 5.34 µg/array, and tips dissolved completely in full-thickness rat skin by 120 s (2 min), indicating a short wear time.
  • After 24 h in ex vivo Franz diffusion studies, 26% of loaded minocycline was deposited in skin versus 18.31% permeated through skin (174.64 ± 12.89 µg vs 123.24 ± 11.62 µg; p = 0.0068).
  • Antibacterial activity was retained: MIC values were <0.146 µg/mL against all tested strains, MBC values were 9.375 µg/mL for S. aureus and 18.75 µg/mL for S. epidermidis and C. acnes, and the largest inhibition zone was against C. acnes at 3.1 cm.

Methods

  • Fabrication used a casting method: tips solution of PLGA (35 mg/mL) and minocycline (25 mg/mL) in DMSO was added to molds, centrifuged at 4500 rpm for 15 min, dried, re-cast, then a PVA:PVP 20/20% w/w baseplate was added and dried.
  • Characterization included manual insertion into full-thickness rat skin, Parafilm® M insertion testing with an Agrosta® Texture Analyzer, mechanical compression testing, UV-spectrophotometric drug content at 347 nm, in vitro PBS dissolution, and ex vivo rat skin dissolution.
  • Ex vivo skin deposition used Franz diffusion cells with full-thickness rat skin, PBS pH 7.4 at 37 ± 1 °C over 24 h; antibacterial testing used agar diffusion, MIC, and MBC against S. aureus ATCC 9144, S. epidermidis ATCC 51625, and C. acnes ATCC 11827; statistics used GraphPad Prism V10 with t-tests/ANOVA and p < 0.05.

Limitations

  • Stated: the paper says further intensive in vivo studies are essential to evaluate safety and efficacy before clinical translation, and future studies will explore stability, expanded antimicrobial experiments, and in vivo safety/efficacy.
  • Evident from the text: all skin insertion, dissolution, and deposition data are from ex vivo rat skin or in vitro setups, with no human or in vivo efficacy/safety data reported.
  • Evident from the text: antibacterial testing used planktonic cultures and standard agar/MIC/MBC methods, not acne biofilm models or the pilosebaceous unit, and drug quantification relied on UV-spectrophotometry rather than a chromatographic method.

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Integrity signals

Registry

Crossref · 10.3390/polym17212912

Cites

44 of 44 references verified0 citation errors · 0 not checkable

Statistics

Nothing to recompute.

Figures

Figure 1 (A). Graphical illustration showing the consequences of treating acne vulgaris using oral minocycline, including bacterial resistance, gut dysbiosis and systemic exposure. (B). Graphical illustration showing the proposed project of developing a MNs transdermal patch loaded with minocycline to provide a sustained topical delivery and minimise the adverse effects associated with oral delivery.
Figure 1 (A). Graphical illustration showing the consequences of treating acne vulgaris using oral minocycline, including bacterial resistance, gut dysbiosis and systemic exposure. (B). Graphical illustration showing the proposed project of developing a MNs transdermal patch loaded with minocycline to provide a sustained topical delivery and minimise the adverse effects associated with oral delivery.CC BY · PubMed Central
Figure 2 PLGA-minocycline tipped microneedles (MNs) preparation method. Tips solution was made of dissolving PLGA (35 mg/mL) and minocycline (25 mg/mL) in DMSO. This solution was used to formulate the tips of the MNs where 40 µL was added using micropipette into MNs moulds. Moulds were centrifuged for 15 min at 4500 rpm to concentrate the solution into the tips. Moulds were left to dry for 24 h at room temperature (RT) then another cast of tips solution with the same volume was performed followed by centrifugation. Moulds were left to dry for 24 h, then an aqueous blend of baseplate formulated from (PVA:PVP 20/20% w/w) was added using 3 mL syringe. Moulds were left to dry for 24 h at RT.
Figure 2 PLGA-minocycline tipped microneedles (MNs) preparation method. Tips solution was made of dissolving PLGA (35 mg/mL) and minocycline (25 mg/mL) in DMSO. This solution was used to formulate the tips of the MNs where 40 µL was added using micropipette into MNs moulds. Moulds were centrifuged for 15 min at 4500 rpm to concentrate the solution into the tips. Moulds were left to dry for 24 h at room temperature (RT) then another cast of tips solution with the same volume was performed followed by centrifugation. Moulds were left to dry for 24 h, then an aqueous blend of baseplate formulated from (PVA:PVP 20/20% w/w) was added using 3 mL syringe. Moulds were left to dry for 24 h at RT.CC BY · PubMed Central
Figure 3 (A). Full thickness rat skin after MNs insertion using manual pressure by thumb pressing for 30 s. (B). Parafilm® M after MNs insertion using Agrosta® Texture Analyzer for 30 s and 32 N. (C). Insertion profile of MNs into Parafilm® M layers using. (D). Microscope images of microneedles before compression force test using Agrosta® Texture Analyzer for 30 s and 32 N. (E). Microscope images of microneedles after compression force test using Agrosta® Texture Analyzer for 30 s and 32 N.
Figure 3 (A). Full thickness rat skin after MNs insertion using manual pressure by thumb pressing for 30 s. (B). Parafilm® M after MNs insertion using Agrosta® Texture Analyzer for 30 s and 32 N. (C). Insertion profile of MNs into Parafilm® M layers using. (D). Microscope images of microneedles before compression force test using Agrosta® Texture Analyzer for 30 s and 32 N. (E). Microscope images of microneedles after compression force test using Agrosta® Texture Analyzer for 30 s and 32 N.CC BY · PubMed Central
Figure 4 Ex vivo skin dissolution study of PLGA-minocycline tipped MNs into full thickness rat skin. (A). After 3 s of application. (B). After 60 s of application. (C). After 120 s of application.
Figure 4 Ex vivo skin dissolution study of PLGA-minocycline tipped MNs into full thickness rat skin. (A). After 3 s of application. (B). After 60 s of application. (C). After 120 s of application.CC BY · PubMed Central
Figure 5 (A). Comparison between minocycline amount that was delivered into rat skin and minocycline amount that was permeated through rat skin after 24 h of PLGA-minocycline tipped microneedles upon performing ex vivo skin deposition study using Franz cells apparatus. (B). Amount of permeated minocycline into reservoir compartment over 24 h of PLGA-minocycline tipped microneedles upon performing ex vivo skin deposition study using Franz cells apparatus.
Figure 5 (A). Comparison between minocycline amount that was delivered into rat skin and minocycline amount that was permeated through rat skin after 24 h of PLGA-minocycline tipped microneedles upon performing ex vivo skin deposition study using Franz cells apparatus. (B). Amount of permeated minocycline into reservoir compartment over 24 h of PLGA-minocycline tipped microneedles upon performing ex vivo skin deposition study using Franz cells apparatus.CC BY · PubMed Central
Figure 6 The antibacterial activity of PLGA-minocycline tipped microneedles and control microneedles (PLGA-DMSO) against (A) S. aureus, (B) S. epidermidis, and (C) C. acnes using agar diffusion method.
Figure 6 The antibacterial activity of PLGA-minocycline tipped microneedles and control microneedles (PLGA-DMSO) against (A) S. aureus, (B) S. epidermidis, and (C) C. acnes using agar diffusion method.CC BY · PubMed Central

Verification

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Citations

Cites

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Research works printed but not linked: 1

  1. Ak, 2019, A comprehensive review of acne vulgaris, J. Clin. Pharm., 1, 17

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Metadata

Authors
Abu Ershaid, J. M., Abudoleh, S. M., Lafi, D. N., & Dahshan, N. A.
Affiliations
  • Department of Applied Pharmaceutical Sciences and Clinical Pharmacy, Faculty of Pharmacy, Isra University, Amman 11622, Jordan
  • Middle East University (JO)
  • Isra University (JO)
Venue
Polymers
Publisher
MDPI AG
Published
2025-10-31
Volume
17
Issue
21
Pages
2912
ISSN
2073-4360 (ISSN-L)
OpenAlex
W4415813462
Cited by
5
References
44
Citations by year
2026: 4 · 2025: 1
FWCI
1.83
Type
journal article
Language
en
Open access
Locations
  • Polymers (publishedVersion, cc-by)
  • Preprints.org (submittedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • PubMed Central (publishedVersion, cc-by)
Funders
Isra University (2023/2022/35-11)
Topics
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advancements in Transdermal Drug Delivery
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
  • Health Sciences › Medicine › Dermatology › Dermatologic Treatments and Research
Keywords
minocycline, microneedles, PLGA, acne treatment, topical drug delivery, skin deposition, antibacterial activity, Staphylococcus aureus, Staphylococcus epidermidis, Propionibacterium acnes, transdermal permeation, casting method, mechanical strength, dissolution behavior

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CoChat. (2026). Citation check: Formulation and Characterization of PLGA Minocycline Microneedles for Enhanced Skin Deposition and Antibacterial Activity in Acne Treatment. https://app.cochat.ai/papers/10.3390/polym17212912
The paper
Abu Ershaid, J. M., Abudoleh, S. M., Lafi, D. N., & Dahshan, N. A. (2025). Formulation and Characterization of PLGA Minocycline Microneedles for Enhanced Skin Deposition and Antibacterial Activity in Acne Treatment. Polymers. https://doi.org/10.3390/polym17212912

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