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皮肤预消融和激光辅助微喷射注射用于深层组织穿透。

Skin pre-ablation and laser assisted microjet injection for deep tissue penetration.

作者信息

Jang Hun-Jae, Yeo Seonggu, Yoh Jack J

机构信息

Department of Mechanical and Aerospace Engineering, Seoul National University, 1 Gwanakro, Gwanakgu, Seoul, Korea, 151-742.

出版信息

Lasers Surg Med. 2017 Apr;49(4):387-394. doi: 10.1002/lsm.22608. Epub 2016 Oct 25.

DOI:10.1002/lsm.22608
PMID:27778355
Abstract

BACKGROUND AND AIMS

For conventional needless injection, there still remain many unresolved issues such as the potential for cross-contamination, poor reliability of targeted delivery dose, and significantly painstaking procedures. As an alternative, the use of microjets generated with Er:YAG laser for delivering small doses with controlled penetration depths has been reported. In this study, a new system with two stages is evaluated for effective transdermal drug delivery. First, the skin is pre-ablated to eliminate the hard outer layer and second, laser-driven microjet penetrates the relatively weaker and freshly exposed epidermis. Each stage of operation shares a single Er:YAG laser that is suitable for skin ablation as well as for the generation of a microjet.

METHODS

In this study, pig skin is selected for quantification of the injection depth based on the two-stage procedure, namely pre-ablation and microjet injection. The three types of pre-ablation devised here consists of bulk ablation, fractional ablation, and fractional-rotational ablation. The number of laser pulses are 12, 18, and 24 for each ablation type. For fractional-rotational ablation, the fractional beams are rotated by 11.25° at each pulse. The drug permeation in the skin is evaluated using tissue marking dyes. The depth of penetration is quantified by a cross sectional view of the single spot injections. Multi-spot injections are also carried out to control the dose and spread of the drug.

RESULTS

The benefits of a pre-ablation procedure prior to the actual microjet injection to the penetration is verified. The four possible combinations of injection are (a) microjet only; (b) bulk ablation and microjet injection; (c) fractional ablation and microjet injection; and (d) fractional-rotational ablation and microjet injection. Accordingly, the total depth increases with injection time for all cases. In particular, the total depth of penetration attained via fractional pre-ablation increased by 8 ∼ 11% and that of fractional-rotational pre-ablation increased by 13 ∼ 33%, when compared with the no pre-ablation or microjet only cases. A noticeable point is that the fraction-rotational pre-ablation and microjet result is comparable to the bulk ablation and microjet result of 11 ∼ 42%. The penetration depth underneath ablated stratum corneum (SC) is also measured in order to verify the pre-ablation effect. The penetration depths for each case are (a) 443 ± 104 µm; (b) 625 ± 98 µm; (c) 523 ± 95 µm; and (d) 595 ± 141 µm for microjet only, bulk ablation and microjet, fractional ablation and microjet, and fractional-rotational ablation and microjet, respectively. This is quite beneficial since any healing time associated with ablation is significantly reduced by avoiding hard-core bulk ablation. Thus the bulk pre-ablation and microjet may well be superseded by the less invasive fractiona-rotational ablation followed by the microjet injection. The density of micro-holes is 1.27 number/mm for fractional ablation and 4.84 number/mm for fractional-rotational ablation. The penetration depths measured underneath the ablated SC are 581 µm (fractional ablation and microjet) and 691 µm (fractional-rotational ablation and microjet).

CONCLUSIONS

Fractional-rotational ablation increases number of micro-holes in a unit area, enabling fast reepithelialization and high drug delivery efficiency. Optimization of system parameters such as ablation time, number of ablations, and injection time will eventually ensure a macromolecule delivery technique with the potential to include vaccines, insulins, and growth hormones, all of which require deeper penetration into the skin. Lasers Surg. Med. 49:387-394, 2017. © 2016 Wiley Periodicals, Inc.

摘要

背景与目的

对于传统的无针注射,仍存在许多未解决的问题,如交叉污染的可能性、靶向给药剂量的可靠性差以及操作过程极为繁琐。作为一种替代方法,已有报道使用铒:钇铝石榴石激光产生的微射流来递送小剂量药物并控制穿透深度。在本研究中,评估了一种新的两阶段系统用于有效的经皮给药。首先,对皮肤进行预消融以去除坚硬的外层,其次,激光驱动的微射流穿透相对较薄且新暴露的表皮。每个操作阶段共享一台适合皮肤消融以及产生微射流的铒:钇铝石榴石激光。

方法

在本研究中,选择猪皮基于预消融和微射流注射的两阶段程序来量化注射深度。这里设计的三种预消融类型包括整体消融、分次消融和分次旋转消融。每种消融类型的激光脉冲数分别为12、18和24。对于分次旋转消融,每个脉冲时分次光束旋转11.25°。使用组织标记染料评估皮肤中的药物渗透。通过单点注射的横截面视图量化穿透深度。还进行多点注射以控制药物的剂量和扩散。

结果

验证了在实际微射流注射之前进行预消融程序对穿透的益处。四种可能的注射组合为:(a)仅微射流;(b)整体消融和微射流注射;(c)分次消融和微射流注射;(d)分次旋转消融和微射流注射。因此,在所有情况下,总深度随注射时间增加。特别是,与无预消融或仅微射流的情况相比,通过分次预消融获得的总穿透深度增加了8%至11%,分次旋转预消融的增加了13%至33%。一个值得注意的点是,分次旋转预消融和微射流的结果与整体消融和微射流的结果相当,为11%至42%。还测量了消融角质层(SC)下方的穿透深度以验证预消融效果。每种情况的穿透深度分别为:(a)仅微射流为443±104μm;(b)整体消融和微射流为625±98μm;(c)分次消融和微射流为523±95μm;(d)分次旋转消融和微射流为595±141μm。这非常有益,因为通过避免硬核整体消融,与消融相关的任何愈合时间都显著减少。因此,整体预消融和微射流很可能被侵入性较小的分次旋转消融继以微射流注射所取代。分次消融的微孔密度为1.27个/mm,分次旋转消融的为4.84个/mm。在消融的SC下方测量的穿透深度分别为581μm(分次消融和微射流)和691μm(分次旋转消融和微射流)。

结论

分次旋转消融增加了单位面积内的微孔数量,实现了快速再上皮化和高药物递送效率。优化系统参数,如消融时间、消融次数和注射时间,最终将确保一种大分子递送技术,有可能包括疫苗、胰岛素和生长激素,所有这些都需要更深地穿透皮肤。《激光外科与医学》49:387 - 394,2017。©2016威利期刊公司

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