TY - JOUR
T1 - PLGA-integrated micro/nanoparticles for cargo delivery and nanomedicine of lung cancer
AU - Kakavandi, Sareh
AU - Zare, Iman
AU - Esmaeilnejad, Narges
AU - Sarhadi, Mohammad
AU - Hheidari, Ali
AU - Shojaei, Shirin
AU - Fatahi, Yousef
AU - Mirshafiei, Mojdeh
AU - Zhang, Mingzhen
AU - Sharifianjazi, Fariborz
AU - Zheng, Kai
AU - Tavamaishvili, Ketevan
AU - Iranpour, Maryam
AU - Kim, Chowon
AU - Zanganeh, Saeed
AU - Thangampillai Senthilkumar, Roshni
AU - Smith, Bryan Ronain
AU - Dinarvand, Rassoul
AU - Rashedi, Hamid
AU - Yu, Meng
AU - Kang, Heemin
AU - Makvandi, Pooyan
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2026/1/5
Y1 - 2026/1/5
N2 - Lung cancer has been the most frequently diagnosed cancer worldwide for several decades. The treatment of lung cancer incurs significant costs for both patients and society, leading to a growing interest in prevention, early detection through screening, and the development of novel therapies. Given the limitations of traditional chemotherapy, the targeted and localized delivery of chemotherapeutics using nanoparticle (NP) carriers to the lungs has emerged as a promising area of research. Poly (lactic-co-glycolic acid) (PLGA) is a key nanotherapeutic that represents a highly promising platform for targeted cancer treatment, particularly for lung cancer. PLGA consists of a family of Food and Drug Administration (FDA)-approved biodegradable polymers that are robust and biocompatible, having been extensively researched as delivery systems for drugs, proteins, and macromolecules, including DNA and RNA. This review examines various PLGA formulations for lung cancer therapy, exploring potential delivery methods such as active targeting, passive targeting, and microarray patches. It also addresses different strategies for drug encapsulation and delivery, and advancements in tumor targeting techniques, including immunotherapy, phototherapy, magnetic targeting, and gene therapy. Furthermore, we highlight the significance of PLGA in the context of lung cancer and metastasis, emphasizing that PLGA-based formulations for the treatment of lung cancer.
AB - Lung cancer has been the most frequently diagnosed cancer worldwide for several decades. The treatment of lung cancer incurs significant costs for both patients and society, leading to a growing interest in prevention, early detection through screening, and the development of novel therapies. Given the limitations of traditional chemotherapy, the targeted and localized delivery of chemotherapeutics using nanoparticle (NP) carriers to the lungs has emerged as a promising area of research. Poly (lactic-co-glycolic acid) (PLGA) is a key nanotherapeutic that represents a highly promising platform for targeted cancer treatment, particularly for lung cancer. PLGA consists of a family of Food and Drug Administration (FDA)-approved biodegradable polymers that are robust and biocompatible, having been extensively researched as delivery systems for drugs, proteins, and macromolecules, including DNA and RNA. This review examines various PLGA formulations for lung cancer therapy, exploring potential delivery methods such as active targeting, passive targeting, and microarray patches. It also addresses different strategies for drug encapsulation and delivery, and advancements in tumor targeting techniques, including immunotherapy, phototherapy, magnetic targeting, and gene therapy. Furthermore, we highlight the significance of PLGA in the context of lung cancer and metastasis, emphasizing that PLGA-based formulations for the treatment of lung cancer.
KW - Active targeting
KW - Lung cancer
KW - Microarray patch
KW - Nanomedicine
KW - PLGA
KW - Passive targeting
KW - Phototherapy
UR - https://www.scopus.com/pages/publications/105022159558
U2 - 10.1016/j.ijpharm.2025.126339
DO - 10.1016/j.ijpharm.2025.126339
M3 - 文献综述
C2 - 41241160
AN - SCOPUS:105022159558
SN - 0378-5173
VL - 687
JO - International Journal of Pharmaceutics
JF - International Journal of Pharmaceutics
M1 - 126339
ER -