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Synthetic biomaterials are relatively easy to prepare and meet quality control requirements during mass production as safe non-living products

unveiled that an eight-arm PEG nanocarrier functionalized with protease-responsive short peptides with oligonucleotides releases DNA barcodes for urinary-based early diagnosis of cancer biomarkers (Fig

In 2000, the first antibodydrug conjugate (ADC) Gemtuzumab ozogamicinMylotarg was approved by the FDA for the treatment of acute myeloid leukemia (AML)

On February 2, 2017, the FDA designated the recall a class II, meaning that exposure might cause temporary health problems, but is unlikely to cause injuries of a serious nature
