© 2016 by World Scientific Publishing Co. Pte. Ltd. The design and synthesis of covalently linked photosensitizer-peptide conjugates are reviewed in this chapter. Peptides of relatively small size (\u3c50 amino acids) are most commonly used for enhancing the photosensitizer targeting specificity, due to their straightforward synthesis and ease of conjugation to photosensitizers. Porphyrin, chlorin and phthalocyanine macrocycles are the most common PDT photosensitizers used in the conjugation reactions to peptides, generally via a low molecular weight linker, following either solution or solid phase protocols. These so-called thirdgeneration photosensitizers have shown increased selectivity for targeting specific cell enzymes or receptors, a...
The thesis is in three parts. Initially, work centred on the development of conjugation technology ...
Antimicrobial peptides (AMPs) are an interesting class of antibiotics characterized by their unique ...
Since the introduction of solid phase peptide synThesis in 1963, peptides and post-translationally m...
Photodynamic therapy (PDT) is a type of cancer therapy that could offer many advantages. One possibl...
Photodynamic therapy (PDT) is a cancer treatment modality that requires three components, namely lig...
Photodynamic therapy is a novel cancer treatment, involving the combination of light, photosensitise...
This thesis presents the contributions we made towards achieving targeted photodynamic therapy (PDT)...
Two series of amphiphilic meso-tetrasubstituted porphyrin conjugates based on 5,10,15,20-tetrakis(3-...
Antimicrobial PhotoDynamic Therapy (APDT) represents a very promising strategy, particularly for t...
Photodynamic therapy (PDT) selectivity and specificity can be improved by binding the photosensitize...
The conjugation of peptides to porphyrins and related tetrapyrrole based macrocycles have extended t...
Photodynamic therapy (PDT) selectivity and specificity can be improved by binding the photosensitize...
The efficacy of new porphyrin amino acid conjugates as photosensitizers for photodynamic therapy (PD...
The objective of this work was to develop methods for preparing novel photosensitizer drugs with a)...
La thérapie photodynamique (PDT) est un type de traitement du cancer qui offre de nombreux avantages...
The thesis is in three parts. Initially, work centred on the development of conjugation technology ...
Antimicrobial peptides (AMPs) are an interesting class of antibiotics characterized by their unique ...
Since the introduction of solid phase peptide synThesis in 1963, peptides and post-translationally m...
Photodynamic therapy (PDT) is a type of cancer therapy that could offer many advantages. One possibl...
Photodynamic therapy (PDT) is a cancer treatment modality that requires three components, namely lig...
Photodynamic therapy is a novel cancer treatment, involving the combination of light, photosensitise...
This thesis presents the contributions we made towards achieving targeted photodynamic therapy (PDT)...
Two series of amphiphilic meso-tetrasubstituted porphyrin conjugates based on 5,10,15,20-tetrakis(3-...
Antimicrobial PhotoDynamic Therapy (APDT) represents a very promising strategy, particularly for t...
Photodynamic therapy (PDT) selectivity and specificity can be improved by binding the photosensitize...
The conjugation of peptides to porphyrins and related tetrapyrrole based macrocycles have extended t...
Photodynamic therapy (PDT) selectivity and specificity can be improved by binding the photosensitize...
The efficacy of new porphyrin amino acid conjugates as photosensitizers for photodynamic therapy (PD...
The objective of this work was to develop methods for preparing novel photosensitizer drugs with a)...
La thérapie photodynamique (PDT) est un type de traitement du cancer qui offre de nombreux avantages...
The thesis is in three parts. Initially, work centred on the development of conjugation technology ...
Antimicrobial peptides (AMPs) are an interesting class of antibiotics characterized by their unique ...
Since the introduction of solid phase peptide synThesis in 1963, peptides and post-translationally m...