Natural Sweetener Stevioside‐Based Dissolving Microneedles Solubilize Minoxidil for the Treatment of Androgenic Alopecia
Junying Zhang, Tianyu Shao, Hailiang Li, Luying Zhu, Lamyaa Albakr, Nial J. Wheate, Lifeng Kang, Chungyong Wu

TL;DR
This study introduces a new method using stevioside to improve minoxidil delivery for treating hair loss, showing better solubility and hair regrowth in animals.
Contribution
A novel use of stevioside as a solubilizing agent and microneedle material to enhance minoxidil delivery for androgenetic alopecia.
Findings
STV increased MXD solubility to 47 mg mL−1, 18 times higher than the control.
MN patches achieved 85% drug release and 18% skin retention in vitro.
Animal studies showed 67.5% coverage of the treatment area by day 35.
Abstract
Androgenetic alopecia (AGA) is a prevalent form of non‐scarring hair loss. Standard treatments, which include minoxidil (MXD) tincture and foam, face challenges due to MXD's water insolubility and poor skin permeability. The result is extended treatment duration and reduced therapeutic effectiveness. This study utilized stevioside (STV), a natural sweetener derived from the Stevia plant, as a novel solubilizing excipient and microneedle (MN) material. A solid dispersion of STV with insoluble drugs is developed and molded into an MN patch. STV significantly increased MXD's solubility to 47 mg mL−1 in water, ≈18 fold higher than the control. STV solubilizes MXD by forming micelles in aqueous solution with a critical micelle concentration of 15 mg mL−1. In vitro skin permeation studies showed cumulative drug release of 85% and 18% skin retention for the MN patch, which indicated excellent…
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Taxonomy
TopicsAdvancements in Transdermal Drug Delivery · Biochemical Analysis and Sensing Techniques · melanin and skin pigmentation
