Pite peg modification

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Peptide drugs have shown great potential in the field of disease diagnosis and treatment due to their high activity, low toxicity and high specificity. However, peptide drugs also have some limitations, such as peptides are easily degraded by enzymes in vivo, resulting in a short duration of efficacy and the need for frequent administration, and some peptides may trigger an immune response, affecting the therapeutic efficacy and side effects, and the peptides are poorly water-soluble, which affects his bioavailability. To overcome these challenges, we have successfully developed polyethylene glycol (PEG) modification to significantly improve the pharmacokinetic properties and increase the stability of peptide drugs. pharmacokinetic properties of peptide drugs, improving their stability and bioavailability.


Technological Breakthroughs

  • Controlled modification: A variety of PEG derivatives and linker arms have been developed to precisely control the length, branching structure and linkage of PEG molecules to optimize the modification effect.
  • Multi-functional modification: Combining PEG modification with other modification technologies (e.g. fatty acid modification, glycosylation modification, etc.) to provide peptide drugs with more functionalities, such as targeting and slow release.
  • Site-specific modification: Through chemical synthesis, PEG molecules are precisely attached to the specific sites of peptides to avoid affecting their active sites.

Technical Advantages

Prolonged half-life: PEG modification can increase the size of peptide molecules, reduce renal filtration, and protect peptides from enzymatic degradation, thus significantly prolonging their half-life.
Reduced immunogenicity: Enmascarar ya epítopos antigénicos jar superficie ar péptido reduce ár inmunogenicidade ne minimiza efectos secundarios.
Mejorada solubilidad: Mejorado ko éxito ar solubilidad ne ar biodisponibilidad fármacos peptídicos.
Mejora nzäm'bu: Mejorar ko éxito nzäm'bu térmico ne química fármacos peptídicos, ne extender ár período almacenamiento.
campos nt'ot'e
tecnología nyokwi ar nyokwi PEG peptídico, tales com:
Ár nte fármacos: Utilizado pa nte xi maa duradera, xí hñets'i'i toxicidad, fármacos peptídicos dirigidos, komongu ar péptidos anticancerígenos, Péptidos antibacterianos, Péptidos analgésicos, etc..
reactivos diagnóstico: pa ár nte reactivos diagnóstico peptídicos altamente sensibles ne específicos, tales como reactivos detección marcador tumoral, reactivos detección virus.
Biomateriales: utilizados pa nte biomateriales péptidos biocompatibles ne funcionales, tales como andamios ingeniería tejido ne sistemas entrega fármacos.

Miao He

Miao He

Research Scientist in Delivery Systems d: Oral peptide delivery, lipid nanoparticle (LNP) encapsulation, cell-penetrating peptides (CPPs), and sustained-release formulations.

Profile: Ya ndu'mi desafíos jar nte fármacos peptídicos residen jar yá cortas ar nzaki media ne ar dificultad ko ar ntsuni oral, y Miao Nu'ä ge 'nar experto líder jar abordar nuya ya hñäki. Nunu̲ posee nt'ot'e ho 'bui ndunthe mfeni jar hwähi ya sistemas entrega peptídicos. Nunu̲ 'bu̲'bya xi centrado jar nte novedosos potenciadores ar permeación ne ar nanosferas pa mejorar significativamente ar biodisponibilidad ar péptidos.

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