# Innovative Nanocarriers: Elastic Aspasomes Loaded with Metformin Hydrochloride for Effective Management of Melasma: In Vitro Studies and Clinical Appraisal

**Authors:** Rofida Albash, Abdurrahman M. Fahmy, Maha H. Ragaie, Shimaa S. Ahmed, Rabab A. El-Gazar, Amira B. Kassem, Manar Adel Abdelbari, Hoda A. Salem, Asmaa Saleh, Shaimaa Mosallam

PMC · DOI: 10.3390/pharmaceutics18030364 · Pharmaceutics · 2026-03-14

## TL;DR

This study develops elastic nanocarriers loaded with metformin to treat melasma, showing effective and stable drug delivery in lab and clinical tests.

## Contribution

The novel use of aspasomes for metformin delivery in melasma treatment is introduced, with optimized formulation and clinical validation.

## Key findings

- Optimized aspasomes showed 87.5% drug entrapment and stable properties over 90 days.
- The cream formulation demonstrated superior clinical efficacy in melasma patients compared to alternatives.
- Sustained drug release and spherical morphology were confirmed through advanced characterization techniques.

## Abstract

Background/Objectives: Aspasomes (ASPs) are composed of ascorbyl palmitate (AP), which has antioxidant activity. The objective of this study was the formulation of aspasomes (ASPs) loaded with metformin hydrochloride (MFC) for the topical treatment of melasma. Methods: MFC-ASPs were prepared using the thin-film method with different amounts of phospholipid and ascorbyl palmitate (AP) in the absence or presence of ethanol surfactant. The prepared formulations were optimized using a D-optimal mixture. The assessed responses included entrapment efficiency (%EE), particle size (PS), polydispersity index (PDI), and zeta potential (ZP). Results: The optimum OASPs, composed of 193.121 mg PC and 30 mg AP, exhibited spherical vesicles with an EE% of 87.50 ± 0.33%, PS of 264.47 ± 0.02 nm, PDI of 0.423 ± 0.001, and ZP of −21.67 ± 0.12 mV. The optimum formula represented a spherical morphology using transmission electron microscopy, along with sustained release behavior compared with MFC. Also, it showed good stability for up to 90 days. Furthermore, a clinical appraisal of patients with melasma confirmed the superiority of the cream compared to the other cream in clinical study. Conclusions: The optimum OASPs present a promising approach for the treatment of melasma topically.

## Linked entities

- **Chemicals:** metformin hydrochloride (PubChem CID 14219), ascorbyl palmitate (PubChem CID 54680660), ethanol (PubChem CID 702)

## Full-text entities

- **Diseases:** Melasma (MESH:D008548)
- **Chemicals:** AP (MESH:C031226), EE (MESH:D004997), MFC (MESH:D008687), phospholipid (MESH:D010743), ethanol (MESH:D000431), PC (MESH:C053518), ASPs (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

54 references — full list in the complete paper: https://tomesphere.com/paper/PMC13029186/full.md

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Source: https://tomesphere.com/paper/PMC13029186