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Delivering drugs specifically to patient neoplasms is a major and ongoing clinical challenge. Function-blocking
monoclonal antibodies were first proposed as cancer therapies nearly four decades ago. The large size of these molecules
hindered their commercial development so that the first antibody or antibody-fragment therapies were only commercialized for
cancer therapeutics and diagnostics 20 years later [1,2]. A classic development during this period, a radiolabelled peptide
analog of somatostatin (SST) was used to target neuroendocrine tumors expressing the SST receptor instead of targeting the
receptor with an antibody [3]. The concept of using a peptide as a targeting moiety for cancer diagnosis and treatment has
since led to current peptide drug developments in both academia and pharmaceutical industries. In addition to cancer
treatments, melanotan 2 peptide that
mimic natural peptide hormones also offer therapeutic opportunities. Synthetic human insulin, for instance, has been long
exemplified for its clinical efficacy for diabetic patients [4].