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Makale detayı · 2024

Effect of Periodate-Induced Cross-linking on Dual Anticancer Drug Release from Poly(2-isopropyl-2-oxazoline)/Tannic Acid-Based Layer-by-Layer Microparticles

ACS Omega

YÖKSİS OpenAlex Açık erişim · gold SJR Q1 JCR Q2 Atıf 5 Yüzdelik 61.7% FWCI 0.62
Yıl
2024
ISSN
2470-1343
Tür
article

Veri kaynağı ayrımı

  • YÖKSİS YÖKSİS makale kaydı
  • OpenAlex OpenAlex zenginleştirmesi (özet, atıf, konular)

Özet

İngilizce (OpenAlex)

High Resolution Image Download MS PowerPoint Slide This study reports, first, on the preparation and cross-linking of multilayers composed of poly(2-isopropyl-2-oxazoline- co -ethyleneimine) (PiPOX-PEI) and tannic acid (TA). PiPOX was synthesized by cationic ring-opening polymerization (CROP) and partially hydrolyzed, yielding a random copolymer PiPOX-PEI. It was then coassembled at the surface with TA using the layer-by-layer (LbL) technique. Multilayers were exposed to NaIO 4 solution to induce covalent bond formation between PEI units of PiPOX-PEI and TA. Cross-linking with NaIO 4 enhanced the stability of the multilayers, especially under basic conditions. Second, the potential of PiPOX-PEI and TA multilayers as a stimuli-responsive dual drug-releasing platform was examined using curcumin (CUR) and doxorubicin (DOX) as model drugs. These drugs were chosen as they can act in a combinatorial manner to increase cell death. The surface of CUR-containing CaCO 3 microparticles was modified with PiPOX-PEI and TA multilayers and postloaded with DOX. We found that LbL particles could release DOX in a pH-responsive manner, whereas temperature-induced release was observed only when the temperature was raised above 40 °C. The DOX and CUR released from the LbL particles could act synergistically on HCT-116 cells. Cross-linking increased the DOX release from LbL particles but decreased the CUR release from the core. Corroborating the release data, the synergy observed with the non-cross-linked particles was lost with the cross-linked particles, and the decrease in the viability of HCT-116 cells was attributed mainly to the release of DOX. Overall, we describe here NaIO 4 -induced cross-linking of PiPOX-PEI/TA LbL films, the effects of pH, temperature, and cross-linking on DOX and CUR release from multilayers, and comparison of the combinatorial effect of DOX and CUR for cross-linked and non-cross-linked LbL microparticles through cell viability assays.

Konular

  • Nanoparticle-Based Drug Delivery
  • Advanced Drug Delivery Systems
  • biodegradable polymer synthesis and properties

Birincil konu Nanoparticle-Based Drug Delivery

Yazarlar

  1. ESMA UĞUR
  2. GÖKÇE TİDİM
  3. DİLARA GÜNDOĞDU
  4. Cemre Alemdar
  5. Goksu Oral
  6. HEPŞEN HAZAL HÜSNÜGİL
  7. SREEPARNA BANERJEE ORTA DOĞU TEKNİK ÜNİVERSİTESİ
  8. İREM EREL GÖKTEPE ORTA DOĞU TEKNİK ÜNİVERSİTESİ
  9. ERKUNT KARABULUT ORTA DOĞU TEKNİK ÜNİVERSİTESİ