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To determine whether a parenterally administered (i.e., tail vein injected) zanamivir-drug conjugate might similarly gain access to virus-infected lung cells, we first prepared a zanamivir-chelate conjugate that binds 99m Tc with high affinity by replacing the DNP moiety of zan-DNP with a chelator of 99m Tc (Fig

J Neuropathol Exp Neurol 49:591599

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