Revolutionizing Cancer Treatment: The Role of Starch-Based Nanoparticles in Targeted Therapy

被引:0
作者
Kapoor, Devesh U. [1 ]
Patel, Geeta [2 ]
Prajapati, Bhupendra G. [2 ]
机构
[1] Dr Dayaram Patel Pharm Coll, Bardoli, Gujarat, India
[2] Ganpat Univ, Shree S K Patel Coll Pharmaceut Educ & Res, Kherva, Gujarat, India
来源
STARCH-STARKE | 2025年 / 77卷 / 05期
关键词
cancer; nanoparticles; passive targeting; starch derivatives; targeted delivery; ACID-HYDROLYSIS; DRUG-DELIVERY; PHYSICOCHEMICAL PROPERTIES; ORAL BIOAVAILABILITY; CROSS-LINKING; PH; NANOCRYSTALS; SIZE; NANOTECHNOLOGY; THERAPEUTICS;
D O I
10.1002/star.202400251
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The biocompatible and biodegradable polysaccharide starch is a great platform for the development of nanoparticles (NPs). Due to its special qualities, which include high stability, low toxicity, and ease of modification, it is a desirable option for the administration of anticancer drugs. Targeted cancer therapy has found a potential carrier in starch-based nanoparticles (SNPs). SNPs can be functionalized with ligands to target cancer cells in particular. These ligands allow for targeted medication delivery by identifying overexpressed receptors on tumor surfaces. SNPs have been studied in relation to chemotherapeutics, siRNAs, and photothermal treatments, among other anticancer agents. They are also used in combination therapy, where their combined targeting of cancer cells improves treatment outcomes. SNPs in cancer treatment are being evaluated in a number of clinical trials. These trials evaluate patient outcomes, safety, and efficacy and offer important information for potential future uses. Regulatory bodies closely monitor various treatments based on NPs. Clinical translation requires an understanding of their safety profiles, biodistribution, and clearance mechanisms. In this review, we examine the potential of SNPs to enhance anticancer medication delivery and treatment efficacy through drug targeting.
引用
收藏
页数:20
相关论文
共 146 条
[71]   Preparation, characterization and utilization of starch nanoparticles [J].
Kim, Hee-Young ;
Park, Sung Soo ;
Lim, Seung-Taik .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2015, 126 :607-620
[72]   Characterization of nanoparticles prepared by acid hydrolysis of various starches [J].
Kim, Hee-Young ;
Lee, Ju Hun ;
Kim, Jong-Yea ;
Lim, Wang-Jin ;
Lim, Seung-Taik .
STARCH-STARKE, 2012, 64 (05) :367-373
[73]   Safety Assessment of Starch Nanoparticles as an Emulsifier in Human Skin Cells, 3D Cultured Artificial Skin, and Human Skin [J].
Kim, So-Yeon ;
Shin, Hye-Young ;
Kim, Jong-Yea ;
Park, Se Jin .
MOLECULES, 2023, 28 (02)
[74]   A Comprehensive Review on Starch-Based Hydrogels: From Tradition to Innovation, Opportunities, and Drawbacks [J].
Koshenaj, Katerina ;
Ferrari, Giovanna .
POLYMERS, 2024, 16 (14)
[75]   Characterization of acid hydrolysis based nano-converted mung bean (Vigna radiata L.) starch for morphological, rheological and thermal properties [J].
Kumari, Suman ;
Yadav, Baljeet S. ;
Yadav, Ritika .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2022, 211 :450-459
[76]   Development and characterization of starch nanoparticles by gamma radiation: Potential application as starch matrix filler [J].
Lamanna, Melisa ;
Morales, Noel ;
Lis Garcia, Nancy ;
Goyanes, Silvia .
CARBOHYDRATE POLYMERS, 2013, 97 (01) :90-97
[77]   Preparation and application of starch nanoparticles for nanocomposites: A review [J].
Le Corre, Deborah ;
Angellier-Coussy, Helene .
REACTIVE & FUNCTIONAL POLYMERS, 2014, 85 :97-120
[78]   Influence of botanic origin and amylose content on the morphology of starch nanocrystals [J].
LeCorre, Deborah ;
Bras, Julien ;
Dufresne, Alain .
JOURNAL OF NANOPARTICLE RESEARCH, 2011, 13 (12) :7193-7208
[79]   Plant-derived exosomal nanoparticles: potential therapeutic for inflammatory bowel disease [J].
Li, De-feng ;
Tang, Qi ;
Yang, Mei-feng ;
Xu, Hao-ming ;
Zhu, Min-zheng ;
Zhang, Yuan ;
Tian, Cheng-mei ;
Nie, Yu-qiang ;
Wang, Jian-yao ;
Liang, Yu-jie ;
Wang, Li-sheng ;
Yao, Jun .
NANOSCALE ADVANCES, 2023, 5 (14) :3575-3588
[80]   Codelivery of DOX and siRNA by folate-biotin-quaternized starch nanoparticles for promoting synergistic suppression of human lung cancer cells [J].
Li, Liangping ;
He, Suoju ;
Yu, Lizhen ;
Elshazly, Ezzat H. ;
Wang, Hui ;
Chen, Kuanmin ;
Zhang, Song ;
Ke, Lixia ;
Gong, Renmin .
DRUG DELIVERY, 2019, 26 (01) :499-508