Poly(N-vinylformamide) Nanogels Capable of pH-Sensitive Protein Release

Hydrogel particles have an historic presence in the field of drug formulation and delivery. Applications of particulate forms of gel materials continue to expand as a result of enhanced control over physicochemical properties including particle size, degradability, and environmental responsiveness. Here, acid-labile poly( N -vinylformamide) (PNVF) nanogels ∼100 nm in diameter were synthesized via inverse emulsion polymerization of N -vinylformamide in the presence of a ketal-containing cross-linker. The dissolution half-life of nanogels proved to be dramatically faster at low pH. Nanogels with a monomer:cross-linker ratio of seven demonstrated a 90 min half-life at pH 5.8 compared to ∼57 h at pH 7.4. Approximately 95% of lysozyme encapsulated in nanogels released over 200 min at pH 5.8 compared to only ∼15% released at pH 7.4. The encapsulation efficiency was moderate with optimal conditions leading to ∼60% encapsulation efficiency. In addition, released lysozyme retained about 50% of the original activity. Large differentials in PNVF nanogel dissolution time and protein release in response to slight changes in pH may ultimately provide a mechanism to selectively deliver macromolecular therapeutics to acidic tissues or intracellular vesicles.