We found that compared to the untreated categories, treatment with 1/10 the MIC of PZA or 1/10 the MIC of INH resulted in a significant decrease in the burden of intracellular M
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The encapsulation of DDA-GSH-AuNCs into PLGA nanoparticles does not alter the well documented biocompatibility of PLGA as evident from similar cellular viability of MCF-7 cells upon exposure to empty PLGA nanoparticles or PLGA nanoparticles encapsulating DDA-GSH-AuNCs in a wide range of nanoparticle concentration (4500 g/mL) as shown in Fig