4.6 Article

Flexible synthesis of cationic peptide-porphyrin derivatives for light-triggered drug delivery and photodynamic therapy

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 14, Issue 48, Pages 11488-11501

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c6ob02135b

Keywords

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Funding

  1. BBSRC at Bath [BB/D0127831, BB/J009164/1, BB0113291, BB/J009318/1]
  2. BBSRC at UCL
  3. University of Bath Faculty of Science
  4. Biotechnology and Biological Sciences Research Council [BB/J009318/1, BB/J009164/1] Funding Source: researchfish
  5. BBSRC [BB/J009318/1, BB/J009164/1] Funding Source: UKRI

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Efficient syntheses of cell-penetrating peptide-porphyrin conjugates are described using a variety of bio-conjugation chemistries. This provides a flexible means to convert essentially hydrophobic tetrapyrolle photosensitisers into amphiphilic derivatives which are well-suited for use in light-triggered drug delivery by photochemical internalisation (PCI) and targeted photodynamic therapy (PDT).

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