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- W4382751347 abstract "The tailored design of drug delivery systems for specific therapeutic agents is a prevailing approach in the field. In this paper, we present a study that highlights the potential of our modified starch, Q-starch, as a universal and adaptable drug delivery carrier for diverse therapeutic agents. We investigate the ability of Q-starch/cargo complexes to target different organelles within the cellular landscape, based on the specific activation sites of therapeutic agents. Plasmid DNA (pDNA), small interfering RNA (siRNA), and phosphatidylinositol (3,4,5)-trisphosphate (PIP3) were chosen as representative therapeutic molecules, acting in the nucleus, cytoplasm, and membrane, respectively. By carrying out comprehensive characterizations, employing dynamic light scattering (DLS), determining the zeta potential, and using cryo-transmitting electron microscopy (cryo-TEM), we reveal the formation of nano-sized, positively charged, and spherical Q-starch complexes. Our results demonstrate that these complexes exhibit efficient cellular uptake, targeting their intended organelles while preserving their physical integrity and functionality. Notably, the intracellular path of the Q-starch/cargo complex is guided by the cargo itself, aligning with its unique biological activity site. This study elucidates the versatility and potency of Q-starch as a versatile drug delivery carrier, paving the way for novel applications offering targeted delivery strategies for potential therapeutic molecules." @default.
- W4382751347 created "2023-07-01" @default.
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- W4382751347 date "2023-06-30" @default.
- W4382751347 modified "2023-09-30" @default.
- W4382751347 title "Cargo-Dependent Targeted Cellular Uptake Using Quaternized Starch as a Carrier" @default.
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- W4382751347 doi "https://doi.org/10.3390/nano13131988" @default.
- W4382751347 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/37446506" @default.
- W4382751347 hasPublicationYear "2023" @default.
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