TY - CHAP
T1 - Extracellular vesicles for ophthalmic and dermal ailments
AU - Datta, Deepanjan
AU - Bandi, Sony Priyanka
AU - Janardhanam, Leela Sai Lokesh
AU - Colaco, Viola
AU - Dhas, Namdev
AU - Anand, Krishnan
AU - Kohli, Kanchan
N1 - Publisher Copyright:
© 2025 Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
PY - 2025/1/1
Y1 - 2025/1/1
N2 - The delivery of peptides across the human eye and skin for disease treatment is challenging due to the presence of the outermost barrier, cornea, and stratum corneum, which are mainly composed of tight junction lipids with a thickness of 10–30µm and 540–560µm, respectively. Various strategies including active and passive approaches have been implemented over the years for enhanced delivery of drug molecules. Extracellular vesicles are low immunogenic, stable, and able to cross biological barriers, which have made them potential carriers favoring the delivery of small and large molecular drugs. These nanovesicles have sizes ranging from 30 to 150nm. Exosomes have been shown to deliver various therapeutic molecules such as curcumin, paclitaxel, doxorubicin, small interfering RNA, microRNAs (miRNAs), and hyaluronidase for the amelioration of various skin ailments. Microneedle (MN) patch is the emerging paradigm to efficiently deliver bioactive payloads. Systemic delivery of drugs can be achieved by the application of micron-sized dissolvable MNs, a minimally invasive approach that offers a painless delivery. Taken together, the fusion of microneedles with exosomes containing bioactive substances such as proteins, DNA, RNA, long noncoding RNA, miRNA, circular RNA proteins, and signaling lipids can be a potential alternative to counteract various ophthalmic and dermal infections.
AB - The delivery of peptides across the human eye and skin for disease treatment is challenging due to the presence of the outermost barrier, cornea, and stratum corneum, which are mainly composed of tight junction lipids with a thickness of 10–30µm and 540–560µm, respectively. Various strategies including active and passive approaches have been implemented over the years for enhanced delivery of drug molecules. Extracellular vesicles are low immunogenic, stable, and able to cross biological barriers, which have made them potential carriers favoring the delivery of small and large molecular drugs. These nanovesicles have sizes ranging from 30 to 150nm. Exosomes have been shown to deliver various therapeutic molecules such as curcumin, paclitaxel, doxorubicin, small interfering RNA, microRNAs (miRNAs), and hyaluronidase for the amelioration of various skin ailments. Microneedle (MN) patch is the emerging paradigm to efficiently deliver bioactive payloads. Systemic delivery of drugs can be achieved by the application of micron-sized dissolvable MNs, a minimally invasive approach that offers a painless delivery. Taken together, the fusion of microneedles with exosomes containing bioactive substances such as proteins, DNA, RNA, long noncoding RNA, miRNA, circular RNA proteins, and signaling lipids can be a potential alternative to counteract various ophthalmic and dermal infections.
UR - https://www.scopus.com/pages/publications/105001896023
UR - https://www.scopus.com/pages/publications/105001896023#tab=citedBy
U2 - 10.1016/B978-0-443-23891-8.00011-1
DO - 10.1016/B978-0-443-23891-8.00011-1
M3 - Chapter
AN - SCOPUS:105001896023
SN - 9780443238925
SP - 283
EP - 345
BT - Extracellular Vesicles for Therapeutic and Diagnostic Applications
PB - Elsevier
ER -