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The mechanistic analysis uncovered that the PEG-b-PSSNa copolymers interact directly with viral particles in a zipper-like method, limiting their particular communication because of the permissive mobile. The antiviral task associated with copolymers is well-correlated aided by the duration of the PSSNa block, indicating that the copolymers' ionic obstructs are biologically energetic. The obstructs of PEG present in copolymers studied don't hinder that discussion. Taking into consideration the practi
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