microneedle array
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2022 ◽  
Author(s):  
Madhu Sharma ◽  
Naresh Mittapelly ◽  
Venkatesh Teja Banala ◽  
Sandeep Urandur ◽  
Shalini Gautam ◽  
...  

2022 ◽  
Vol 32 (3) ◽  
pp. 2270022
Author(s):  
Muamer Dervisevic ◽  
Maria Alba ◽  
Li Yan ◽  
Mehmet Senel ◽  
Thomas R. Gengenbach ◽  
...  

2021 ◽  
Vol 23 (12) ◽  
pp. 401-416
Author(s):  
Snehal S. Patil ◽  
◽  
Nikita S. Patil ◽  
Umesh C. Suryawanshi ◽  
Mr. Rohan R. Vakhariya ◽  
...  

Drug delivery through the skin by transdermal patches has a long history. Subsequent growth of transdermal science proved prominent utility of transdermal systems meant for passive diffusion of the drug. It was followed by the development of Iontophoresis and Sonophoresis based transdermal delivery systems. Microneedle array has now caught attention of the investigators owing to its immense utility in transdermal delivery of very large molecules with ionic and hydrophilic nature. In this technical note, we present the current scenario, applications, and recent advances in microneedle array-based delivery of the most critical molecules through the skin. The application of microneedle has widely been investigated, and these technologies are being developed for the delivery of bio-therapeutics, biomacromolecules, insulin, growth hormones, immunobiologicals, proteins, siRNA and peptides. Potential of microneedles to transform the global transdermal market is highlighted in terms of the success rate of the microneedle technologies in clinical trials reaching to the global market. The arrival of the commercial microneedle-based products in the market is highly anticipated as they have potential to portray remarkable impact on clinical medicine in near future.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Pritsana Sawutdeechaikul ◽  
Silada Kanokrungsee ◽  
Thanyapat Sahaspot ◽  
Kamonwan Thadvibun ◽  
Wijit Banlunara ◽  
...  

AbstractDelivering bioactive compounds into skin tissue has long been a challenge. Using ex vivo porcine and rat skins, here we demonstrate that a detachable dissolvable microneedle (DDMN) array, a special dissolvable microneedle that allows needle detachment from the base within 2 min post administration, can effectively embed a model compound into epidermis and dermis. Diffusion of the compound from the needle embedding sites to the nearby skin tissue is demonstrated at various post administration periods. The relationship between the time that a conventional dissolvable microneedle array is left on skin without needle detachment from the base and the degree of skin surface abrasion at each microneedle penetration spot is also demonstrated on skin of human volunteers. Co-loading glutathione with vitamin C (vitC) can stabilize vitC in the DDMN. DDMN loaded with vitC and glutathione can help erasing post-acne-hyperpigmentation spots.


2021 ◽  
pp. 2103449
Author(s):  
Shun Yao ◽  
Yuetong Wang ◽  
Junjie Chi ◽  
Yunru Yu ◽  
Yuanjin Zhao ◽  
...  

Author(s):  
Kai Takeuchi ◽  
Nobuyuki Takama ◽  
Kirti Sharma ◽  
Oliver Paul ◽  
Patrick Ruther ◽  
...  

2021 ◽  
pp. 2100874
Author(s):  
SeungHyun Park ◽  
Yong Jae Kim ◽  
Sanghyun Park ◽  
Hyeonaug Hong ◽  
JiYong Lee ◽  
...  

Author(s):  
Ben Creelman ◽  
Collrane Frivold ◽  
Sierra Jessup ◽  
Gene Saxon ◽  
Courtney Jarrahian

AbstractMicroneedle array patch (MAP) technology is a promising new delivery technology for vaccines and pharmaceuticals, yet due to several differing and novel production methods, barriers to full-scale manufacturing exist. PATH conducted a manufacturing readiness assessment and follow-up interviews to identify both the current manufacturing readiness of the industry as well as how readiness varies by developer type and MAP type. Follow-up interviews identified barriers the industry faces in reaching full manufacturing readiness, including the perceived regulatory and investment risk of manufacturing MAPs at scale due to quality requirements and control methods, uncertain sterility requirements, lack of standard production methods (especially around dissolvable MAP drying methods), and the lack of available contract manufacturing organizations with MAP manufacturing capabilities. A Regulatory Working Group has been established to identify and address critical quality issues specific to MAP manufacturing with the aim of providing developers insight into what will be expected for MAP product approvals. Standardizing MAP production equipment and automatic, visual quality control could reduce the overall investment risk to developers and contract manufacturing organizations in pursuing pilot-scale manufacturing capabilities and ultimately lower barriers to the scale-up of full medical MAP product lines. Graphical abstract


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