Advanced Skin Delivery of L-Arginine: Design, Characterization, and Anti-Aging Efficacy of Optimized Cubosomal Nanocarriers.

The purpose of this study was to develop a L-arginine-loaded cubosomal nanocarrier cream for topical anti-aging application. Glyceryl Monooleate and Poloxamer 407 cubosomes effectively encapsulated L-arginine, resulting in a nanosized structure (∼34.7 nm) with high entrapment efficiency (71.67 ± 0.81%). Optimal drug content (96 ± 0.08%), ideal viscosity (19,666 cps), and skin-compatible pH (6.4 ± 0.3) were obtained when incorporated into a cream base containing almond oil, Cosmacol ELI, and Sepineo P600. Formulation physiochemical compatibility was confirmed by FTIR and DSC study, sustained drug release (78.92% over 6 hours) shown by <i>in vitro</i> release study. Reduced TNF-α expression indicated that the formulation did not elicit any pro-inflammatory response, whereas cell viability was found to be above 80%. Reduced MMP-1 and increased collagen I gene levels demonstrated anti-aging efficacy. Over a six-month period, stability studies confirmed that there was no phase separation. Overall, the cubosomal cream showed outstanding entrapment, stability, safety, and anti-aging potential, offering a promising non-invasive cosmeceutical approach for skin rejuvenation.

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Publication Details

Journal
Pharmaceutical Development and Technology
Published
2026-03-28
DOI
https://doi.org/10.1080/10837450.2026.2652978
Primary Topic
Advancements in Transdermal Drug Delivery
Type
article
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article

Advanced Skin Delivery of L-Arginine: Design, Characterization, and Anti-Aging Efficacy of Optimized Cubosomal Nanocarriers.

Ashwin Kuchekar, Rutuja Vinchurkar
Pharmaceutical Development and Technology
Advancements in Transdermal Drug Delivery
article

Advanced Skin Delivery of L-Arginine: Design, Characterization, and Anti-Aging Efficacy of Optimized Cubosomal Nanocarriers.

Ashwin Kuchekar, Rutuja Vinchurkar
article en

Abstract

The purpose of this study was to develop a L-arginine-loaded cubosomal nanocarrier cream for topical anti-aging application. Glyceryl Monooleate and Poloxamer 407 cubosomes effectively encapsulated L-arginine, resulting in a nanosized structure (∼34.7 nm) with high entrapment efficiency (71.67 ± 0.81%). Optimal drug content (96 ± 0.08%), ideal viscosity (19,666 cps), and skin-compatible pH (6.4 ± 0.3) were obtained when incorporated into a cream base containing almond oil, Cosmacol ELI, and Sepineo P600. Formulation physiochemical compatibility was confirmed by FTIR and DSC study, sustained drug release (78.92% over 6 hours) shown by <i>in vitro</i> release study. Reduced TNF-α expression indicated that the formulation did not elicit any pro-inflammatory response, whereas cell viability was found to be above 80%. Reduced MMP-1 and increased collagen I gene levels demonstrated anti-aging efficacy. Over a six-month period, stability studies confirmed that there was no phase separation. Overall, the cubosomal cream showed outstanding entrapment, stability, safety, and anti-aging potential, offering a promising non-invasive cosmeceutical approach for skin rejuvenation.

Pharmaceutical Development and Technology
MIT World Peace University (IN)
Openalex Percentile: Top 4%
Advancements in Transdermal Drug Delivery
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Advanced Skin Delivery of L-Arginine: Design, Characterization, and Anti-Aging Efficacy of Optimized Cubosomal Nanocarriers. — Ashwin Kuchekar, Rutuja Vinchurkar · Pharmaceutical Development and Technology (2026) | TGRS Research Map | TGRS