Article(id=1322631201970573433, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1322631195876242221, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.17.011, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1773244800000, receivedDateStr=2026-03-12, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1793269451849, onlineDateStr=2026-10-29, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1793269451849, onlineIssueDateStr=2026-10-29, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1793269451849, creator=13701087609, updateTime=1793269451849, updator=13701087609, issue=Issue{id=1322631195876242221, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='17', pageStart='6661', pageEnd='7072', issueExtLink='null', onlineDate='null', pubDate='1789142400000', pubDateStr='2026-09-12', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1793269450396, creator='13701087609', updateTime=1793269538381, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1322631565008556693, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1322631195876242221, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1322631565008556694, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1322631195876242221, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=6779, endPage=6792, ext={EN=ArticleExt(id=1322631202561970299, articleId=1322631201970573433, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Preparation of cedrol nanosuspension and its pharmacodynamic study on treatment of androgenetic alopecia, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To enhance the hair follicle-targeted delivery efficiency of cedrol, a cedrol nanosuspension (Ce-NS) was prepared. The formulation and process parameters were optimized, the physicochemical properties were characterized, and its therapeutic efficacy in the treatment of androgenetic alopecia (AGA) was evaluated. Methods Ce-NS was prepared using a solvent-antisolvent precipitation method. Based on single-factor experiments, particle size and polydispersity index (PDI) were selected as evaluation parameters to optimize the formulation and process variables using the Box-Behnken design-response surface methodology (BBD-RSM). The physicochemical characteristics and storage stability of the formulation were determined by dynamic light scattering (DLS). Invitro transdermal performance was evaluated using a Franz diffusion cell system. Morphological characteristics were examined by scanning electron microscopy (SEM) to assess the accumulation of nanocrystals within hair follicles. An AGA model was established in C57BL/6 mice. Hematoxylin-eosin (HE) staining and immunohistochemical analysis of dorsal skin tissues were performed to evaluate the invivo hair growth-promoting efficacy. Results The optimal formulation parameters were as follows: cedrol mass concentration 7.5 mg/mL, sodium dodecyl sulfate (SDS) 170 mg, hydroxypropyl methylcellulose (HPMC) 130 mg, and a polyethylene glycol (PEG) 400-to-water phase ratio of 1∶12. The process parameters included a dropping rate of 20 mL/min, stirring speed of 10 000 r/min, and shearing time of 5 min. The prepared Ce-NS exhibited a mean particle size of (434.47 ± 9.90) nm, a PDI of 0.232 ± 0.005, and a ζ potential of (&8722;15.20 ± 1.15) mV. The experimental values were in good agreement with the predicted values of the model. Ce-NS remained stable for 90 days at room temperature. Invitro transdermal studies showed that the skin retention of Ce-NS within 24 h reached (74.38 ± 3.90) μg/cm2, which was 4.1-fold higher than that of the raw drug group, while no cedrol was detected in the receptor medium. SEM observation of skin sections confirmed the accumulation of cedrol nanocrystals within hair follicles. Pharmacodynamic evaluation demonstrated that, compared with the model group, Ce-NS significantly promoted hair regeneration in AGA model mice, increased hair follicle density and hair length, decreased androgen receptor (AR) expression in dorsal skin tissue, and upregulated the expression of Ki67 and β-catenin. Conclusion Ce-NS was successfully prepared using a green preparation process and exhibited stable physicochemical properties. The formulation significantly enhanced the skin retention and follicular targeting of cedrol, demonstrating promising therapeutic potential for androgenetic alopecia. The underlying mechanism may be associated with the downregulation of androgen signaling and activation of the Wnt/β-catenin pathway., authors=GUAN Lu1,2, JI Yixiao1,2, WANG Xian3, LEI Wanfeng3, LI Ping3, LU Shan1,2, GUO Yujie1,2, HONG Yi1,2, authorsList=GUAN Lu, JI Yixiao, WANG Xian, LEI Wanfeng, LI Ping, LU Shan, GUO Yujie, HONG Yi, authorCompany=1 Research Center for Pharmaceutical Preparation, School of Pharmacy, Hubei University of Chinese Medicine, Wuhan 430065, China; 2 Hubei Shizhen Laboratory, Wuhan 430065, China; 3 Wuhan Runhe Bio-pharmaceutical Co., Ltd., Wuhan 430040, China, correspAuthors=null, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1322631202465501306, articleId=1322631201970573433, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=雪松醇纳米混悬剂的制备及其治疗雄激素性脱发的药效学研究, columnId=1304140189132149234, journalTitle=中草药, columnName=药剂与工艺, runingTitle=null, highlight=null, articleAbstract=目的 为提高雪松醇的毛囊靶向递送效率,制备雪松醇纳米混悬剂(cedrol-nanosuspension,Ce-NS),进行处方工艺优化、理化性质表征,并评价其治疗雄激素性脱发(androgenetic alopecia,AGA)的药效。方法 采用溶剂-反溶剂沉淀法制备Ce-NS,在单因素实验的基础上,以粒径大小和多分散指数(polydispersity index,PDI)为考察指标,应用Box-Behnken设计-响应面法(Box-Behnken design-response surface methodology,BBD-RSM)对处方工艺参数进行系统优化。利用动态光散射(dynamic light scattering,DLS)对制剂的理化性质及贮藏稳定性进行表征。通过Franz扩散池评价体外透皮能力,采用扫描电子显微镜(scanning electron microscope,SEM)进行形态学研究并评估毛囊中纳米晶体的积累,建立C57BL/6小鼠AGA模型,对其背部皮肤组织进行苏木精-伊红(HE)染色、免疫组织化学染色评价其促进体内生发药效。结果 确定最优处方工艺为雪松醇的质量浓度为7.5 mg/mL,十二烷基硫酸钠(sodium dodecyl sulfate,SDS)用量为170 mg,羟丙基甲基纤维素(hydroxypropyl methylcellulose,HPMC)用量为130 mg,聚乙二醇(polyethylene glycol,PEG)400与水相的比例为1∶12;滴加速度为20 mL/min,搅拌速度为10 000 r/min,剪切时间为5 min。所得Ce-NS粒径为(434.47±9.90)nm,PDI为0.232±0.005,ζ电位为(-15.20±1.15)mV,实测值与模型预测值拟合良好。Ce-NS在室温下放置90 d,稳定性良好。体外透皮结果显示,24 h内Ce-NS的皮肤滞留量为(74.38±3.90)μg/cm²,较原料药组显著提高4.1倍,且在接收液中未检出。SEM扫描皮肤切片证实了雪松醇纳米晶体在毛囊内的积累。药效学实验表明,与模型组相比,Ce-NS能有效促进AGA模型小鼠毛发再生,并显著增加毛囊数量与毛发长度,且小鼠背部皮肤组织中的雄激素受体(androgen receptor,AR)表达水平下降,而Ki-67 抗原(Ki-67 antigen,Ki67)、β-连环蛋白(Beta-catenin,β-catenin)表达水平升高。结论 采用绿色工艺成功制备了Ce-NS,且理化性质稳定,并能显著提高雪松醇在皮肤中的滞留量以及成功靶向到毛囊,对AGA表现出良好的治疗潜力,其作用机制可能与降低雄激素水平和促进Wnt/β-连环蛋白信号通路(Wnt/β-catenin)传导有关。, authors=官鹭1,2, 戢逸潇1,2, 王线3, 雷万锋3, 李平3, 卢山1,2, 郭瑜婕1,2, 洪怡1,2, authorsList=官鹭, 戢逸潇, 王线, 雷万锋, 李平, 卢山, 郭瑜婕, 洪怡, authorCompany=1 湖北中医药大学药学院 药物制剂中心, 湖北 武汉 430065; 2 湖北时珍实验室, 湖北 武汉 430065; 3 武汉润禾生物医药有限公司, 湖北 武汉 430040, correspAuthors=洪怡, authorNote=官鹭: 官鹭(1999—),女,硕士研究生,研究方向为药物制剂新技术研究。E-mail:862756829@qq.com, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, 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orderTime=1789142400000, fullTextJson=null, articleText=null, reference=Premanand A, Reena Rajkumari B. Androgen modulation of Wnt/β-catenin signaling in androgenetic alopecia [J]. Arch Dermatol Res, 2018, 310(5): 391-399. Krysiak R, Kowalcze K, Marek B, et al. The impact of levothyroxine on thyroid autoimmunity and hypothalamic-pituitary-thyroid axis activity in men with autoimmune hypothyroidism and early-onset androgenetic alopecia [J]. Endokrynol Pol, 2021, 72(5): 498-504. Gao H, Zhang J Y, Zhao L J, et al. Synthesis and application of clinically approved small-molecule drugs targeting androgen receptor [J]. Bioorg Chem, 2024, 143: 106998. Devjani S, Ezemma O, Kelley K J, et al. Androgenetic alopecia: Therapy update [J]. Drugs, 2023, 83(8): 701-715. Randolph M, Tosti A. Oral minoxidil treatment for hair loss: A review of efficacy and safety [J]. J Am Acad Dermatol, 2021, 84(3): 737-746. 汤陆扬, 卢小鸾, 杨敏, 等. 雪松醇的合成应用及其药理作用研究进展[J]. 化学试剂, 2021, 43(1): 48-54. Özek G, Schepetkin I A, Yermagambetova M, et al. Innate immunomodulatory activity of cedrol, a component of essential oils isolated from Juniperus species [J]. Molecules, 2021, 26(24): 7644. Sakhaee M H, Sayyadi S A H, Sakhaee N, et al. Cedrol protects against chronic constriction injury-induced neuropathic pain through inhibiting oxidative stress and inflammation [J]. Metab Brain Dis, 2020, 35(7): 1119-1126. Adamantidi T, Grabrucker A M, Tsoupras A. Targeting platelet activating factor signaling for therapeutic benefits in neurodegenerative disorders [J]. Front Biosci, 2025, 30(4): 38300. Luo F, Ling Y, Li D S, et al. Characterization of a sesquiterpene cyclase from the glandular trichomes of Leucosceptrum canum for sole production of cedrol in Escherichia coli and Nicotiana benthamiana [J]. Phytochemistry, 2019, 162: 121-128. Prajapat P, Sharma P K, Dwivedi S, et al. A systematic review on nanosuspension and its advancements [J]. Int J Pharmö 2023, 14(4): 17-24. Chavda V P, Vaghela D A, Solanki H K, et al. Nanosuspensions: A new era of targeted therapeutics [J]. J Drug Deliv Sci Technol, 2025, 105: 106613. Karakucuk A, Tort S, Han S, et al. Etodolac nanosuspension based gel for enhanced dermal delivery: In vitro and in vivo evaluation [J]. J Microencapsul, 2021, 38(4): 218-232. Lai Y X, Wu J C, Tan T H, et al. Engineered exosomes co-delivering EGF and FGF ameliorate androgenetic alopecia in a mouse model [J]. Int J Nanomed, 2026, 21: 572518. Junge A, Radonjic-Hoesli S, Bossart S, et al. Contact dermatitis caused by topical minoxidil: Allergy or just irritation [J]. Acta Derm Venereol, 2025, 105: 42401. 田凯, 许丹, 卢迪, 等. 阿苯达唑纳米混悬剂的研制及其评价[J]. 中国兽药杂志, 2022, 56(7): 60-67. Petrovic S, Bita B, Barbinta-Patrascu M E. Nanoformulations in pharmaceutical and biomedical applications: Green perspectives [J]. Int J Mol Sci, 2024, 25(11): 5842. Jacob S, Kather F S, Boddu S H S, et al. Nanosuspension innovations: Expanding horizons in drug delivery techniques [J]. Pharmaceutics, 2025, 17(1): 136. Soisuwan S, Teeranachaideekul V, Wongrakpanich A, et al. Impact of uncharged and charged stabilizers on in vitro drug performances of clarithromycin nanocrystals [J]. Eur J Pharm Biopharm, 2019, 137: 68-76. Rachmawati H, Al Shaal L, Müller R H, et al. Development of curcumin nanocrystal: Physical aspects [J]. J Pharm Sci, 2013, 102(1): 204-214. 曹秋芳, 蒋青香, 郑玲玲, 等. 基于质量源于设计理念结合模糊层次分析法-熵权法优化羟丙甲基纤维素改善栀子水提物可压性研究[J]. 中草药, 2024, 55(16): 5448-5458. Shobha U, Aditi B, Vaishali K. Effect of various stabilizers on the stability of lansoprazole nanosuspension prepared using high shear homogenization: Preliminary investigation [J]. J Appl Pharm Sci, 2021(9): 85-92. Wang Y H, Qin W H, Yang Y J, et al. A study on the processing technology for Rhizoma Coptidis [J]. BMC Biotechnol, 2022, 22(1): 3. Du L X, Lu H L, Xiao Y F, et al. Preparation, characterization and in vivo pharmacokinetic study of ginsenoside Rb1-PLGA nanoparticles [J]. Sci Rep, 2023, 13(1): 18472. Kumar P, Kumar V, Sahoo S, et al. Enhancing alopecia areata management: Nanocrystal-driven strategy for targeting hair follicles [J]. Int J Pharm, 2025, 675: 125557. Heydari S, Barzegar-Jalali M, Heydari M, et al. The impact of particle size of nanostructured lipid carriers on follicular drug delivery: A comprehensive analysis of mouse and human hair follicle penetration [J]. Bioimpacts, 2024, 14(6): 30243. Gu Y T, Bian Q, Zhou Y J, et al. Hair follicle-targeting drug delivery strategies for the management of hair follicle-associated disorders [J]. Asian J Pharm Sci, 2022, 17(3): 333-352. Madaan A, Verma R, Singh A T, et al. Review of hair follicle dermal papilla cells as in vitro screening model for hair growth [J]. Int J Cosmet Sci, 2018, 40(5): 429-450. Lin X Y, Zhu L, He J. Morphogenesis, growth cycle and molecular regulation of hair follicles [J]. Front Cell Dev Biol, 2022, 10: 899095.)
Preparation of cedrol nanosuspension and its pharmacodynamic study on treatment of androgenetic alopecia
GUAN Lu1,2, JI Yixiao1,2, WANG Xian3, LEI Wanfeng3, LI Ping3, LU Shan1,2, GUO Yujie1,2, HONG Yi1,2
Affiliations
1 Research Center for Pharmaceutical Preparation, School of Pharmacy, Hubei University of Chinese Medicine, Wuhan 430065, China; 2 Hubei Shizhen Laboratory, Wuhan 430065, China; 3 Wuhan Runhe Bio-pharmaceutical Co., Ltd., Wuhan 430040, China
Objective To enhance the hair follicle-targeted delivery efficiency of cedrol, a cedrol nanosuspension (Ce-NS) was prepared. The formulation and process parameters were optimized, the physicochemical properties were characterized, and its therapeutic efficacy in the treatment of androgenetic alopecia (AGA) was evaluated. Methods Ce-NS was prepared using a solvent-antisolvent precipitation method. Based on single-factor experiments, particle size and polydispersity index (PDI) were selected as evaluation parameters to optimize the formulation and process variables using the Box-Behnken design-response surface methodology (BBD-RSM). The physicochemical characteristics and storage stability of the formulation were determined by dynamic light scattering (DLS). Invitro transdermal performance was evaluated using a Franz diffusion cell system. Morphological characteristics were examined by scanning electron microscopy (SEM) to assess the accumulation of nanocrystals within hair follicles. An AGA model was established in C57BL/6 mice. Hematoxylin-eosin (HE) staining and immunohistochemical analysis of dorsal skin tissues were performed to evaluate the invivo hair growth-promoting efficacy. Results The optimal formulation parameters were as follows: cedrol mass concentration 7.5 mg/mL, sodium dodecyl sulfate (SDS) 170 mg, hydroxypropyl methylcellulose (HPMC) 130 mg, and a polyethylene glycol (PEG) 400-to-water phase ratio of 1∶12. The process parameters included a dropping rate of 20 mL/min, stirring speed of 10 000 r/min, and shearing time of 5 min. The prepared Ce-NS exhibited a mean particle size of (434.47 ± 9.90) nm, a PDI of 0.232 ± 0.005, and a ζ potential of (&8722;15.20 ± 1.15) mV. The experimental values were in good agreement with the predicted values of the model. Ce-NS remained stable for 90 days at room temperature. Invitro transdermal studies showed that the skin retention of Ce-NS within 24 h reached (74.38 ± 3.90) μg/cm2, which was 4.1-fold higher than that of the raw drug group, while no cedrol was detected in the receptor medium. SEM observation of skin sections confirmed the accumulation of cedrol nanocrystals within hair follicles. Pharmacodynamic evaluation demonstrated that, compared with the model group, Ce-NS significantly promoted hair regeneration in AGA model mice, increased hair follicle density and hair length, decreased androgen receptor (AR) expression in dorsal skin tissue, and upregulated the expression of Ki67 and β-catenin. Conclusion Ce-NS was successfully prepared using a green preparation process and exhibited stable physicochemical properties. The formulation significantly enhanced the skin retention and follicular targeting of cedrol, demonstrating promising therapeutic potential for androgenetic alopecia. The underlying mechanism may be associated with the downregulation of androgen signaling and activation of the Wnt/β-catenin pathway.
GUAN Lu, JI Yixiao, WANG Xian, LEI Wanfeng, LI Ping, LU Shan, GUO Yujie, HONG Yi.
Preparation of cedrol nanosuspension and its pharmacodynamic study on treatment of androgenetic alopecia[J].
Chinese Traditional and Herbal Drugs,
2026
, 57
(17)
: 6779
-6792
.
DOI: 10.7501/j.issn.0253-2670.2026.17.011
基金
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湖北省经济和信息化厅第五批中小微企业“科技副总”对接项目 (61)
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Premanand A, Reena Rajkumari B. Androgen modulation of Wnt/β-catenin signaling in androgenetic alopecia [J]. Arch Dermatol Res, 2018, 310(5): 391-399. Krysiak R, Kowalcze K, Marek B, et al. The impact of levothyroxine on thyroid autoimmunity and hypothalamic-pituitary-thyroid axis activity in men with autoimmune hypothyroidism and early-onset androgenetic alopecia [J]. Endokrynol Pol, 2021, 72(5): 498-504. Gao H, Zhang J Y, Zhao L J, et al. Synthesis and application of clinically approved small-molecule drugs targeting androgen receptor [J]. Bioorg Chem, 2024, 143: 106998. Devjani S, Ezemma O, Kelley K J, et al. Androgenetic alopecia: Therapy update [J]. Drugs, 2023, 83(8): 701-715. Randolph M, Tosti A. Oral minoxidil treatment for hair loss: A review of efficacy and safety [J]. J Am Acad Dermatol, 2021, 84(3): 737-746. 汤陆扬, 卢小鸾, 杨敏, 等. 雪松醇的合成应用及其药理作用研究进展[J]. 化学试剂, 2021, 43(1): 48-54. Özek G, Schepetkin I A, Yermagambetova M, et al. Innate immunomodulatory activity of cedrol, a component of essential oils isolated from Juniperus species [J]. Molecules, 2021, 26(24): 7644. Sakhaee M H, Sayyadi S A H, Sakhaee N, et al. Cedrol protects against chronic constriction injury-induced neuropathic pain through inhibiting oxidative stress and inflammation [J]. Metab Brain Dis, 2020, 35(7): 1119-1126. Adamantidi T, Grabrucker A M, Tsoupras A. Targeting platelet activating factor signaling for therapeutic benefits in neurodegenerative disorders [J]. Front Biosci, 2025, 30(4): 38300. Luo F, Ling Y, Li D S, et al. Characterization of a sesquiterpene cyclase from the glandular trichomes of Leucosceptrum canum for sole production of cedrol in Escherichia coli and Nicotiana benthamiana [J]. Phytochemistry, 2019, 162: 121-128. Prajapat P, Sharma P K, Dwivedi S, et al. A systematic review on nanosuspension and its advancements [J]. Int J Pharmö 2023, 14(4): 17-24. Chavda V P, Vaghela D A, Solanki H K, et al. Nanosuspensions: A new era of targeted therapeutics [J]. J Drug Deliv Sci Technol, 2025, 105: 106613. Karakucuk A, Tort S, Han S, et al. Etodolac nanosuspension based gel for enhanced dermal delivery: In vitro and in vivo evaluation [J]. J Microencapsul, 2021, 38(4): 218-232. Lai Y X, Wu J C, Tan T H, et al. Engineered exosomes co-delivering EGF and FGF ameliorate androgenetic alopecia in a mouse model [J]. Int J Nanomed, 2026, 21: 572518. Junge A, Radonjic-Hoesli S, Bossart S, et al. Contact dermatitis caused by topical minoxidil: Allergy or just irritation [J]. Acta Derm Venereol, 2025, 105: 42401. 田凯, 许丹, 卢迪, 等. 阿苯达唑纳米混悬剂的研制及其评价[J]. 中国兽药杂志, 2022, 56(7): 60-67. Petrovic S, Bita B, Barbinta-Patrascu M E. Nanoformulations in pharmaceutical and biomedical applications: Green perspectives [J]. Int J Mol Sci, 2024, 25(11): 5842. Jacob S, Kather F S, Boddu S H S, et al. Nanosuspension innovations: Expanding horizons in drug delivery techniques [J]. Pharmaceutics, 2025, 17(1): 136. Soisuwan S, Teeranachaideekul V, Wongrakpanich A, et al. Impact of uncharged and charged stabilizers on in vitro drug performances of clarithromycin nanocrystals [J]. Eur J Pharm Biopharm, 2019, 137: 68-76. Rachmawati H, Al Shaal L, Müller R H, et al. Development of curcumin nanocrystal: Physical aspects [J]. J Pharm Sci, 2013, 102(1): 204-214. 曹秋芳, 蒋青香, 郑玲玲, 等. 基于质量源于设计理念结合模糊层次分析法-熵权法优化羟丙甲基纤维素改善栀子水提物可压性研究[J]. 中草药, 2024, 55(16): 5448-5458. Shobha U, Aditi B, Vaishali K. Effect of various stabilizers on the stability of lansoprazole nanosuspension prepared using high shear homogenization: Preliminary investigation [J]. J Appl Pharm Sci, 2021(9): 85-92. Wang Y H, Qin W H, Yang Y J, et al. A study on the processing technology for Rhizoma Coptidis [J]. BMC Biotechnol, 2022, 22(1): 3. Du L X, Lu H L, Xiao Y F, et al. Preparation, characterization and in vivo pharmacokinetic study of ginsenoside Rb1-PLGA nanoparticles [J]. Sci Rep, 2023, 13(1): 18472. Kumar P, Kumar V, Sahoo S, et al. Enhancing alopecia areata management: Nanocrystal-driven strategy for targeting hair follicles [J]. Int J Pharm, 2025, 675: 125557. Heydari S, Barzegar-Jalali M, Heydari M, et al. The impact of particle size of nanostructured lipid carriers on follicular drug delivery: A comprehensive analysis of mouse and human hair follicle penetration [J]. Bioimpacts, 2024, 14(6): 30243. Gu Y T, Bian Q, Zhou Y J, et al. Hair follicle-targeting drug delivery strategies for the management of hair follicle-associated disorders [J]. Asian J Pharm Sci, 2022, 17(3): 333-352. Madaan A, Verma R, Singh A T, et al. Review of hair follicle dermal papilla cells as in vitro screening model for hair growth [J]. Int J Cosmet Sci, 2018, 40(5): 429-450. Lin X Y, Zhu L, He J. Morphogenesis, growth cycle and molecular regulation of hair follicles [J]. Front Cell Dev Biol, 2022, 10: 899095.