Fractional erbium-doped yttrium aluminum garnet laser-assisted drug delivery: impact of triamcinolone acetonide formulation on drug permeation.

IF 5.7 3区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Drug Delivery and Translational Research Pub Date : 2024-12-24 DOI:10.1007/s13346-024-01771-y
Premrutai Thitilertdecha, Teerapat Wannawittayapa, Panyapat Buranaporn, Cyryl Rae Benjamine Santiago Rejuso-Kalbit, Rosalyn Kupwiwat, Poonsin Poungpairoj, Varangkana Tantithavorn, Nattawat Onlamoon, Woraphong Manuskiatti
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Abstract

Ablative fractional laser-assisted drug delivery has gained attention as a promising method for enhancing dermal drug absorption and improving therapeutic outcomes in dermatological conditions, particularly for hypertrophic and keloid scars. However, despite the growing number of clinical trials and case reports supporting its efficacy, there remains a scarcity of robust evidence on the topical bioavailability and dermato-pharmacokinetics of drugs in human subjects. This study aimed to examine the enhancement of triamcinolone acetonide (TAC) bioavailability following treatment with a fractional Erbium-Doped Yttrium Aluminum Garnet (Er: YAG) laser. Stratum corneum (SC) uptake and transport of TAC from 0.1% TAC cream and 10 mg/mL TAC solution/suspension with and without the laser pre-treatment were determined through tape stripping method for SC collection. TAC therein was quantified by an ultra-performance liquid chromatography coupled with photodiode array (UPLC-PDA) detection. TAC from both formulations without laser assistance was percutaneously absorbed within 6 h and TAC was delivered out from the solution to the SC remarkably higher. When the skin was pre-treated with the laser, permeability of TAC from the solution was escalated by 5 folds. TAC distribution profiles in the SC also confirmed this increased drug uptake, mainly the outer skin layers. On the other hand, amounts of absorbed TAC and their distribution patterns from the cream remained unchanged and low. No adverse events and unbearable pain were observed throughout the experiments. The fractional Er: YAG laser enhanced the dermal absorption of TAC, but this effect was confined to the solution formulation, with no significant improvement seen in the cream. This finding highlights the critical role that drug formulation plays in laser-assisted drug delivery. Moreover, factors such as drug selection, laser type, and optimal laser settings may also impact the efficacy of this approach and require further exploration.

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分数掺铒钇铝石榴石激光辅助给药:曲安奈德制剂对药物渗透的影响。
作为一种有前途的方法,消融分数激光辅助给药已经引起了人们的关注,因为它可以增强皮肤药物吸收,改善皮肤疾病的治疗效果,特别是对于肥厚性和瘢痕疙瘩疤痕。然而,尽管越来越多的临床试验和病例报告支持其有效性,但仍然缺乏关于药物在人体中的局部生物利用度和皮肤药代动力学的有力证据。本研究旨在研究分数掺铒钇铝石榴石(Er: YAG)激光治疗后曲安奈德(TAC)生物利用度的增强。采用胶带剥离法测定激光预处理前后角质层(SC)对0.1% TAC乳膏和10 mg/mL TAC溶液/混悬液中TAC的吸收和转运情况。采用超高效液相色谱-光电二极管阵列(UPLC-PDA)法对其中的TAC进行定量分析。在没有激光辅助的情况下,两种配方的TAC在6小时内被经皮吸收,并且TAC从溶液中递送到SC的量明显更高。当用激光对皮肤进行预处理时,溶液中TAC的渗透率提高了5倍。TAC在SC中的分布也证实了这种增加的药物摄取,主要是外层皮肤。另一方面,从乳膏中吸收TAC的量及其分布模式保持不变且较低。在整个实验过程中没有观察到不良事件和无法忍受的疼痛。分数Er: YAG激光增强了TAC的真皮吸收,但这种效果仅限于溶液配方,在乳霜中没有明显的改善。这一发现强调了药物配方在激光辅助给药中所起的关键作用。此外,药物选择、激光类型和最佳激光设置等因素也可能影响该方法的疗效,需要进一步探索。
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来源期刊
Drug Delivery and Translational Research
Drug Delivery and Translational Research MEDICINE, RESEARCH & EXPERIMENTALPHARMACOL-PHARMACOLOGY & PHARMACY
CiteScore
11.70
自引率
1.90%
发文量
160
期刊介绍: The journal provides a unique forum for scientific publication of high-quality research that is exclusively focused on translational aspects of drug delivery. Rationally developed, effective delivery systems can potentially affect clinical outcome in different disease conditions. Research focused on the following areas of translational drug delivery research will be considered for publication in the journal. Designing and developing novel drug delivery systems, with a focus on their application to disease conditions; Preclinical and clinical data related to drug delivery systems; Drug distribution, pharmacokinetics, clearance, with drug delivery systems as compared to traditional dosing to demonstrate beneficial outcomes Short-term and long-term biocompatibility of drug delivery systems, host response; Biomaterials with growth factors for stem-cell differentiation in regenerative medicine and tissue engineering; Image-guided drug therapy, Nanomedicine; Devices for drug delivery and drug/device combination products. In addition to original full-length papers, communications, and reviews, the journal includes editorials, reports of future meetings, research highlights, and announcements pertaining to the activities of the Controlled Release Society.
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