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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].