Evidence map›Paper›PMID 41781552›Full record

ArticleAAPS PharmSciTech2026

Bi-Layered Tablets as a Novel Platform for Wound Healing and Synergistic Combination Therapy.

Kranthi Gattu, Andrew Ramirez, Hua Zhu, Ketan Patel, Shanzhi Wang, Hyunah Cho

Abstract read
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In one paragraph

Article in AAPS PharmSciTech, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Kranthi Gattu *Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, Queens, New York, 11439, USA.ORCID http://orcid.org/0009-0008-3199-6724
Andrew Ramirez *Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, Queens, New York, 11439, USA.ORCID http://orcid.org/0000-0002-4841-534X
Hua ZhuDepartment of Surgery, The Ohio State University Wexner Medical Center, Columbus, Ohio, 43210, USA.ORCID http://orcid.org/0000-0001-7136-7326
Ketan PatelDepartment of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, Queens, New York, 11439, USA.ORCID http://orcid.org/0000-0001-8252-0234
Shanzhi WangDepartment of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, Queens, New York, 11439, USA. wangs1@stjohns.edu.ORCID http://orcid.org/0000-0002-7068-0756
Hyunah ChoDepartment of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, Fairleigh Dickinson University, Florham Park, New Jersey, 07932, USA. hyunahc@fdu.edu.ORCID http://orcid.org/0000-0001-7150-4191

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Effective management of acute wounds, particularly those caused by burns and trauma, remains a significant clinical challenge. Conventional formulations, such as ointments, creams, and hydrogels, often face challenges related to stability, portability, and patient compliance. To address these limitations, we developed a novel bi-layered skin tablet system using direct compression for immediate application to topical wounds. The upper protective layer contains konjac glucomannan as a gelling agent and oleic acid as a permeability enhancer. The lower therapeutic layer includes a synergistic combination of clindamycin hydrochloride (CLC), benzalkonium chloride (BKC), and recombinant human mitsugumin 53 (rhMG53), a membrane repair protein. rhMG53 was repurposed for acute wound healing at a reduced dosage to maintain therapeutic efficacy while improving cost efficiency. The formulation was optimized to achieve controlled release of rhMG53 for wound repair and of CLC and BKC for antibacterial activity. The synergistic interaction between CLC and BKC (Index 1.2) enhanced broad-spectrum antibacterial efficacy. The prepared tablets underwent in-vitro testing for hardness, swelling index, content uniformity, drug release, and stability. The rhMG53 containing formulation demonstrated consistent drug loading (98.5%, RSD < 6%), prolonged release, and effective wound healing in cell-based tests. The tablet form improves portability, stability, and ease of application compared with conventional remedies. This bi-layered skin tablet system represents a promising therapeutic strategy for acute wound management, particularly in emergency and military settings where lightweight, ready-to-use treatments are critically needed.

Indexed as

TabletsWound HealingAnti-Bacterial AgentsChemistry, PharmaceuticalClindamycinDelayed-Action PreparationsDrug LiberationDrug SynergismHumansAnti-Bacterial AgentsClindamycinDelayed-Action PreparationsTabletsantibiotics synergybi-layered tabletcontrolled releaseMG53would healing

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.