Effect of process variables on in vitro characteristics of clindamycin phosphate loaded PLGA nanoparticles in dental bone regeneration and 3D characterization studies using nano-CT


Ilhan M., KILIÇARSLAN M., ORHAN K.

JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, cilt.76, 2022 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 76
  • Basım Tarihi: 2022
  • Doi Numarası: 10.1016/j.jddst.2022.103710
  • Dergi Adı: JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Biotechnology Research Abstracts, EMBASE
  • Anahtar Kelimeler: Clindamycin phosphate, Nanoparticle, Bone regeneration, PLGA, Nano-CT, Periodontal drug delivery, VIVO EVALUATION, DELIVERY, DRUG, RELEASE, MICROPARTICLES, MICROSPHERES, SCAFFOLDS, FORMULATION, PCL
  • Ankara Üniversitesi Adresli: Evet

Özet

Bone tissue surrounding the teeth may be lost due to traumatic, pathological, or physiological reasons, which can result in tooth loss. Therefore, studies in the field of dental surgery have focused on preventing bone loss around the teeth as well as bone regeneration. In the present work, clindamycin phosphate loaded polymeric nano -particles were developed as a local drug delivery system to promote alveolar bone regeneration. The effects of PVA concentration, drug/polymer ratio, inner phase content, polymer type, and pH of the external water phase on the characterization of nanoparticles were investigated by determining the encapsulation efficiency, particle size and size distribution, surface morphology, 3D structure, drug release, and release kinetics of formulations. Encapsulation efficiency was highly dependent on PVA concentration and pH of the external water phase. The mean particle size decreased with the decrease in molecular weight of PLGA. Although using clindamycin phosphate, a water soluble drug, sustained release was achieved for up to 3 months for all formulations. This study revealed that nano-CT visualization is critical in explaining the effects of process parameters on the characterization of nanoparticles. With the 3D images obtained through nano-CT, the internal and external structural properties of the nanoparticles were obtained both visually and quantitatively. The findings of nano -CT imaging that simultaneously determine the 3D structure, size, volume and porosity of nanoparticles were promising for further studies unlike SEM. The differences of internal structural properties between the nano -particles prepared using PCL and PLGA, which could not be distinguished using SEM images, were revealed through nano-CT imagery. Thus, thanks to the 2D and 3D images obtained by nano-CT, it was determined that densely capsular nanoparticles were formed using PCL, and nanoparticles in a matrix structure were formed with PLGA. In addition, the use of nano-CT scanning was particularly effective in interpreting the dissolution rate. Imaging the internal structures of the nanoparticles gave interpretable results in the formulation choices made in this study.