A New Paradigm for Numerical Simulation of Microneedle-Based Drug Delivery Aided by Histology of Microneedle-Pierced Skin

透皮 药物输送 计算机科学 生物医学工程 扩散 软件 药品 简单(哲学) 材料科学 纳米技术 工程类 物理 医学 认识论 精神科 药理学 哲学 程序设计语言 热力学
作者
Tao Han,Diganta Bhusan Das
出处
期刊:Journal of Pharmaceutical Sciences [Elsevier BV]
卷期号:104 (6): 1993-2007 被引量:9
标识
DOI:10.1002/jps.24425
摘要

Microneedle (MN) is a relatively recent invention and an efficient technology for transdermal drug delivery (TDD). Conventionally, mathematical models of MNs drug delivery define the shape of the holes created by the MNs in the skin as the same as their actual geometry. Furthermore, the size of the MN holes in the skin is considered to be either the same or a certain fraction of the length of the MNs. However, the histological images of the MN-treated skin indicate that the real insertion depth is much shorter than the length of the MNs and the shapes may vary significantly from one case to another. In addressing these points, we propose a new approach for modeling MN-based drug delivery, which incorporates the histology of MN-pierced skin using a number of concepts borrowed from image processing tools. It is expected that the developed approach will provide better accuracy of the drug diffusion profile. A new computer program is developed to automatically obtain the outline of the MNs-treated holes and import these images into computer software for simulation of drug diffusion from MN systems. This method can provide a simple and fast way to test the quality of MNs design and modeling, as well as simulate experimental studies, for example, permeation experiments on MN-pierced skin using diffusion cell. The developed methodology is demonstrated using two-dimensional (2D) numerical modeling of flat MNs (2D). However, the methodology is general and can be implemented for three dimensional (3D) MNs if there is sufficient number of images for reconstructing a 3D image for numerical simulation. Numerical modeling for 3D geometry is demonstrated by using images of an ideal 3D MN. The methodology is not demonstrated for real 3D MNs, as there are not sufficient numbers of images for the purpose of this paper.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
积极的初瑶完成签到,获得积分10
刚刚
1秒前
xiaowan完成签到,获得积分10
1秒前
1秒前
xin完成签到,获得积分10
1秒前
彩色从雪完成签到,获得积分10
2秒前
昔我往矣完成签到 ,获得积分10
2秒前
colddie完成签到,获得积分10
2秒前
jiangnan完成签到,获得积分10
2秒前
寒彻骨ii完成签到,获得积分10
2秒前
睡个好觉完成签到,获得积分10
2秒前
lxh发布了新的文献求助10
3秒前
cyuan完成签到,获得积分10
3秒前
3秒前
小宋完成签到,获得积分10
3秒前
文艺的鲜花完成签到 ,获得积分10
3秒前
3秒前
火火发布了新的文献求助10
3秒前
3秒前
小透明发布了新的文献求助10
3秒前
lily完成签到,获得积分10
3秒前
青柚子完成签到,获得积分10
4秒前
李健的小迷弟应助十六采纳,获得10
4秒前
shawnho完成签到,获得积分10
4秒前
多情怜蕾完成签到,获得积分10
5秒前
顺利翠萱完成签到,获得积分10
5秒前
5秒前
33完成签到,获得积分10
5秒前
牦牛发布了新的文献求助10
5秒前
Seasun发布了新的文献求助10
5秒前
雪白的雪完成签到,获得积分10
5秒前
乐乐完成签到,获得积分10
5秒前
6秒前
6秒前
6秒前
芥末发布了新的文献求助10
6秒前
Moto_Fang发布了新的文献求助10
7秒前
迷人听蓉完成签到,获得积分10
7秒前
7秒前
JamesPei应助YMH采纳,获得10
7秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Prompt Engineering for Clinicians: Harnessing AI in Everyday Medical Practice 600
University Physics for the Life Sciences 500
REAL-WORLD EFFICACY AND GENOMIC LANDSCAPE OF POLATUZUMA VEDOTIN-BASED FIRST-LINE THERAPY IN DIFFUSE LARGE B-CELL LYMPHOMA: A FOCUS ON TP53 MUTATIONS AND TREATMENT RESPONSE 500
Handbook of Luminescence Dating 500
Safety Pharmacology 500
《KNN基无铅压电陶瓷电学性能优化与物理机理研究》 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 计算机科学 化学工程 生物化学 物理 内科学 复合材料 催化作用 光电子学 物理化学 电极 细胞生物学 基因 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6952022
求助须知:如何正确求助?哪些是违规求助? 8636246
关于积分的说明 18312339
捐赠科研通 6394755
什么是DOI,文献DOI怎么找? 3082285
关于科研通互助平台的介绍 2127728
邀请新用户注册赠送积分活动 2059159