The synthesis of peptide-conjugated poly(2-ethyl-2-oxazoline)-b-poly(L-lactide) (PEtOx-b-PLA) polymeric systems through the combination of controlled polymerization techniques and click reactions

Ozkose U. U., Gulyuz S., PARLAK KHALİLY M., ÖZÇUBUKÇU S., BOZKIR A., TAŞDELEN M. A., ...Daha Fazla

JOURNAL OF APPLIED POLYMER SCIENCE, cilt.138, sa.17, 2021 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 138 Sayı: 17
  • Basım Tarihi: 2021
  • Doi Numarası: 10.1002/app.50286
  • Dergi Adı: JOURNAL OF APPLIED POLYMER SCIENCE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, PASCAL, Aerospace Database, Applied Science & Technology Source, Biotechnology Research Abstracts, Chemical Abstracts Core, Chimica, Communication Abstracts, Compendex, INSPEC, Metadex, Civil Engineering Abstracts
  • Anahtar Kelimeler: amphiphilic block copolymer, copper&#8208, catalysed azide&#8208, alkyne cycloaddition, peptide grafting, Poly(oxazoline), poly(l&#8208, lactide), thiol&#8208, ene click chemistry, RING-OPENING POLYMERIZATION, AMPHIPHILIC DIBLOCK, COPOLYMERS, DRUG, MICELLES, DELIVERY, DESIGN, ENCAPSULATION, BEHAVIOR
  • Ankara Üniversitesi Adresli: Evet

Özet

To optimize the therapeutic effect of pharmaceutical agents, drug delivery systems tailored from FDA-approved polymers like poly(L-lactide) (PLA) is an effective strategy. Because of their hydrophobic character, these systems greatly suffer from reduced circulation time thus, amphiphilic block copolymers became favorable to overcome this limitation. Of them, poly(oxazoline)-b-poly(L-lactide) are of choice as poly(oxazoline) (PEtOx) is compatible, biodegradable, while exhibiting minimum cytotoxicity. To tailor selective drug targeting drug delivery systems, whereby their selectivity for tumor tissues is maximized, these polymers should be decorated with so-called tumor-homing agents, such as antibodies, peptides and so forth. To this respect, we designed a new block copolymer, allyl-poly(2-ethyl-2-oxazoline)-b-poly(L-lactide) allyl-(PEtOx-b-PLA) and its subsequent conjugation to tumor-homing peptides, peptide-18, and peptide-563 at the terminal position. In this manuscript, we report our synthetic route to obtain this building block and its conjugation to tumor-homing agents.