This dissertation presents the development of a biomaterial-based nanoparticle system designed to integrate precise targeting with controllable drug release. To achieve precise targeting, F(ab’)₂ antibody fragments were conjugated to biodegradable...
This dissertation presents the development of a biomaterial-based nanoparticle system designed to integrate precise targeting with controllable drug release. To achieve precise targeting, F(ab’)₂ antibody fragments were conjugated to biodegradable and biocompatible poly(lactic-co-glycolic acid) (PLGA) nanoparticles. This design allows independent control of two functional dimensions: the surface layer, which determines ligand orientation, density, and binding specificity; and the polymeric core, which controls drug encapsulation level, composition, and release kinetics. Through this dual-level modulation, the system enables alignment between biological targeting and pharmacodynamic profiles.
In Chapter 2, a controlled head-to-head comparison between F(ab’)₂-conjugated nanoparticles and whole-IgG–conjugated nanoparticles was
performed under strictly matched physicochemical conditions, including size and zeta potential. Following intravenous administration in mice, F(ab’)₂-conjugated nanoparticles exhibited superior in vivo targeting efficiency, with markedly increased accumulation in circulating and splenic target immune cells. These findings establish the fragment-based conjugation strategy as a more effective targeting approach than whole-antibody–based formulations.
In Chapter 3, the platform was applied to an inflammatory lung disease model to evaluate therapeutic utility. A sequential treatment strategy targeting neutrophil extracellular traps (NETs) and neutrophil elastase (NE) was developed using a combination of an inhalable DNase I–polydopamine nanoparticle to reduce NET formation, followed by intravenous delivery of sivelestat-loaded anti-Ly6G F(ab’)₂ nanoparticles to suppress neutrophil hyperactivation. This sequential approach decreased neutrophil burden, lowered NET/NE-associated biomarkers, improved lung function, and reduced fibrotic remodeling as indicated by hydroxyproline levels, while maintaining a favorable safety profile.
In chapter 4, the system was extended to oncology using anti-PD-L1 F(ab’)₂-modified nanoparticles loaded with doxorubicin. These nanoparticles achieved enhanced intratumoral accumulation, improved cytotoxicity, and superior tumor growth inhibition at matched drug doses. Immune profiling showed increased effector T cell activation and decreased exhaustion markers, indicating beneficial reprogramming of the tumor immune microenvironment. Additionally, systemic toxicity markers in cardiac and splenic tissues were reduced, demonstrating an improved therapeutic window.
Collectively, this study developed modular nanoplatform that maintains precise antigen recognition through F(ab’)₂ ligands while independently controlling drug release behavior. By decoupling targeting from release, the system allows disease-specific optimization of therapeutic performance. The platform demonstrated applicability in both immune and tumor models, simultaneously improving selectivity, efficacy, and safety. Furthermore, it extends the core design principles of antibody therapeutics into a clinically validated nanoparticle system, providing a conceptual framework that bridges antibody based therapy with biomaterials based drug delivery technology.