TY - JOUR
T1 - Recent Developments in Nanoparticle Synthesis for Targeted Drug Delivery
T2 - A Comprehensive Review
AU - Abbasi, Ali
AU - Rahbar-Kelishami, Ahmad
AU - Zareie, Matin
AU - Padrela, Luis
N1 - Publisher Copyright:
© 2025 Wiley-VCH GmbH.
PY - 2025/8
Y1 - 2025/8
N2 - In pharmaceutical and chemical engineering, addressing newly discovered drugs’ solubility and bioavailability challenges is imperative. Nanoparticle (NP)-based drug delivery systems have emerged as a promising strategy to enhance these compounds’ solubility and overall therapeutic efficacy while minimizing adverse effects. This review presents a comprehensive analysis of synthesis methods for drug-loaded NPs that effectively address solubility limitations. Various chemical synthesizing methods, such as nanoprecipitation, solvent evaporation, and supercritical fluid techniques, are discussed, along with physical methods, including milling, spray-drying, and freeze-drying. Each synthesis approach is evaluated in terms of its underlying principles, advantages, and limitations. Additionally, the importance of NP characterization techniques, such as evaluating drug loading, particle size, and surface properties, is emphasized. Understanding these synthesis methods is crucial for optimizing NP formulations to achieve desired drug delivery outcomes, including improved solubility, controlled release profiles, and targeted delivery to specific sites in the body.
AB - In pharmaceutical and chemical engineering, addressing newly discovered drugs’ solubility and bioavailability challenges is imperative. Nanoparticle (NP)-based drug delivery systems have emerged as a promising strategy to enhance these compounds’ solubility and overall therapeutic efficacy while minimizing adverse effects. This review presents a comprehensive analysis of synthesis methods for drug-loaded NPs that effectively address solubility limitations. Various chemical synthesizing methods, such as nanoprecipitation, solvent evaporation, and supercritical fluid techniques, are discussed, along with physical methods, including milling, spray-drying, and freeze-drying. Each synthesis approach is evaluated in terms of its underlying principles, advantages, and limitations. Additionally, the importance of NP characterization techniques, such as evaluating drug loading, particle size, and surface properties, is emphasized. Understanding these synthesis methods is crucial for optimizing NP formulations to achieve desired drug delivery outcomes, including improved solubility, controlled release profiles, and targeted delivery to specific sites in the body.
KW - Drug delivery
KW - Nano-drug synthesis
KW - Nanomedicine
KW - Nanoparticle
KW - Pharmaceutical
UR - https://www.scopus.com/pages/publications/105009773583
U2 - 10.1002/cben.70015
DO - 10.1002/cben.70015
M3 - Review article
AN - SCOPUS:105009773583
SN - 2196-9744
VL - 12
JO - ChemBioEng Reviews
JF - ChemBioEng Reviews
IS - 4
M1 - e70015
ER -