Cite this article as Sawasdee K, Choksawad P, Pimcharoen S, Prapainop K. Development of size‐tunable polymeric nanoparticles for drug delivery applications. Global Health Management Journal. 2017; 1(2): 31‐6. Global Health Management Journal www.publications.inschool.id PUBLISHED BY Original Research Article ISSN 2580-9296 (ONLINE) Development of size-tunable polymeric nanoparticles for drug delivery applications Komkrich Sawasdee 1 , Ployphailin Choksawad 1 , Sopida Pimcharoen 2 , Kanlaya Prapainop 1,* 1 Department of Biochemistry, Faculty of Science, Mahidol University, Bangkok, Thailand. 2 Samsenwittayalai School, Rama VI Road, Bangkok, Thailand. *Corresponding author. Email: kanlaya.pra@mahidol.edu ARTICLE INFO ABSTRACT Article history: Submitted 16 October 2017 Accepted 27 October 2017 Background: Poly lactide-co-glycolide (PLGA) nanoparticles (NPs) have been widely used in drug delivery applications because of their excellent properties such as biocompatibility, and biodegradability along with the ability to deliver hydrophobic drugs, increase drug bioavailability and improve drug absorption to targeted cells in both oral and parenteral administrations. The PLGA NPs can be synthesized using an emulsion solvent evaporation method. Each parameter during synthesis plays a role in the formation of nanoparticles and can affect NP size; important factors for successful development of a drug delivery system. Aims: The aim of this study was to prepare different sizes of PLGA NPs by investigation of four factors (molecular weight, MW) of PLGA, emulsifier concentrations, organic solvent type and power of ultrasonication) involved in PLGA nanoparticle synthesis. Methods: PLGA nanoparticles were prepared by an emulsion solvent evaporation method. Size and size distribution were analyzed by dynamic light scattering and polydispersity index (PdI). Results: The effect of four parameters: PLGA MW, emulsifier concentrations, solvent types, and amplitude of ultrasonication on PLGA NPs preparation were evaluated. Changing one parameter results in different sizes of PLGA NPs that varied from 150- 300 nm. PdI which is an indicator for determination of size distribution of NPs, varied with an overall value <0.2. Conclusion: MW of PLGA polymer, emulsifier concentration, type of organic solvent and power of ultrasonication affect the size and size distribution of PLGA NPs. Keywords: Drug delivery Polymeric nanoparticles Tunable size of nanoparticles © 2017 Publications of Yayasan Aliansi Cendekiawan Indonesia Thailand This is an open access following Creative Commons License Deed – Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) INTRODUCTION Cancer is a worldwide health problem with millions of people suffering from this disease in both economically developed countries and developing countries [1]. The current strategies for treatment of cancer include surgery, radiation, immunotherapy or chemotherapy. The chemotherapeutic drug is administered intravenously can spread to accumulate in off- targeted tissues or organs leading to undesirable side effects. To solve these problems, anti-cancer drug loaded nanoparticles have gained extensive attention to use as an effective drug delivery system to specific target sites [1, 2]. Polymeric NPs have unique properties including stability, biocompatibility and ease of surface chemistry modification [3, 4]. Therefore these nanoparticles have been used in drug delivery