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From Screening to Optimization: Strategic Implementation of Design of Experiments (DOE) for Robust Nanoparticle Formulation.

Created on 27 Aug 2026

Authors

Ritu Gupta, Mahua Sarkar, Huan Xie

Published in

Polymers. Volume 18. Issue 16. Aug 21, 2026. Epub Aug 21, 2026.

Abstract

Design of experiments (DOE) offers a powerful, systematic framework for optimizing nanoparticle (NP) formulations by replacing inefficient one-factor-at-a-time (OFAT) methods. By enabling the simultaneous evaluation of multiple variables, DOE uncovers critical factor interactions and identifies true global optima-critical for quality-by-design approaches. Despite its potential for systematic innovation, DOE remains underutilized in nanomedicine due to its perceived complexity; this review provides a practical roadmap to bridge the gap between statistical theory and robust NP optimization. It provides a practical overview of DOE concepts, including factor selection, design choice, graphical interpretation of results (perturbation/contour plots), model validation (regression analysis and ANOVA), and numerical optimization via desirability function (D). Common pitfalls and best-practice strategies are discussed to support reliable model building and decision-making. A practical case study on poly(lactic-co-glycolic acid) (PLGA) NPs illustrates a multistage workflow: utilizing Taguchi screening to isolate key factors, followed by central composite design (CCD), for precise surface mapping. Numerical optimization using Design-Expert® software maximized EE% (highest importance) within size/zeta ranges, yielding optimal conditions (5 mg drug amount, 4 mL aqueous volume; D = 0.961). Confirmation runs (EE 41.2%, NP size 124 nm, zeta potential -15 mV) validated predictions (EE 47.6%, NP size 133 nm, zeta potential -17.2 mV), confirming model reliability. Ultimately, by bridging conceptual foundations with practical implementation, this review aims to encourage broader adoption of DOE, particularly among emerging formulation scientists, and serves as a roadmap to accelerate scalable NP development, fostering data-driven innovation and improving efficiency in nanomedicine research. Moreover, future integration of artificial intelligence (AI) and artificial neural networks (ANNs) with DOE will drive a predictive, data-driven approach to NP optimization-accelerating robust, scalable, and regulatory-ready nanomedicine development with fewer experiments.

PMID:
42655314
Bibliographic data and abstract were imported from PubMed on 27 Aug 2026.

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