NON-CATIONIC SOFT POLYPHENOL NANOCAPSULES FOR EFFECTIVE SYSTEMIC DELIVERY OF SMALL INTERFERING RNA (siRNA) FOR CANCER TREATMENT
AssigneePurdue Research Foundation
InventorsYoon Yeo, Hyungjun Kim
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AssigneePurdue Research Foundation
InventorsYoon Yeo, Hyungjun Kim
Estimating the term…
The present disclosure generally relates to a composition matter and a method for cancer treatment. In particular, a composition of soft, non-cationic nanocapsules, termed Nanosac, for systemic delivery of siRNA. Nanosac is produced by sequential attachment of siRNA and polydopamine on a sacrificial MSN core, followed by removal of the MSN. Encapsulating siRNA in the capsules, Nanosac avoids the issues common to cationic gene carriers, such as toxicity and non-specific protein binding while protecting siRNA from RNase. Nanosac entered tumor cells by caveolae-mediated endocytosis, likely via albumin recruited from serum, trafficked to the cytosol, and silenced target genes.
A method of manufacturing soft, non-cationic nanocapsules (Nanosac) for in vivo delivery of a therapeutic compound (TC) comprising:
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A composition of soft, non-cationic nanocapsules (Nanosac) useful for in vivo delivery of a therapeutic compound (TC) manufactured according to the steps of
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A method of intratumoral delivery of a therapeutic compound (TC) to a patient comprising preparing a dosage form of a composition of soft, non-cationic nanocapsules (Nanosac), wherein the Nanosac is manufactured according to a process of:
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Dependencies are inferred from the claim text.