Comparison of SDS and TritonX-100 effects on cell removing of bovine spongy bone for using in bone replacements

Message:
Article Type:
Research/Original Article (دارای رتبه معتبر)
Abstract:
Background

Preserving the biological structure of the initial nature of cancellous bone could prepare it for a proper scaffold for successful bone tissue engineering. Moreover, it is vital to eliminate the cells belonging to its bed to increase its biocompatibility and reduce their immunological responses.

Methods

In this study, Chemical methods were used for decellularization of three-dimensional scaffolds made from spongy calfchr('39')s pelvic bone. For this purpose, the bone samples which were cut from calf pelvis bone were degreased, and then their cells were removed through chemical (sodium dodecyl sulfate (SDS) and TritonX-100 with different concentrations) method. The samples were characterized by hematoxylin and eosin staining, trichrome staining, and optical and scanning electron microscope. In the end, to ensure the absence of toxic substances in the scaffold, a cell toxicity test was conducted.

Results

The results show that the decellularized samples with TritonX-100 of 2% and combining solution of 3% TritonX-100 and 4% SDS respectively (T3S4) can substitute for damaged cancellous bone tissue. The results indicated that calf pelvic spongy bone tissue, as a xenograft that has undergone decellularization with SDS and Triton x-100 chemical solutions, can produce an appropriate scaffold for bone tissue engineering. The natural bone tissue with preservation of collagen fibers and the presence of porosity in its structure can provide a suitable environment for tissue regeneration..

Conclusion

The results suggested that T3S4-acellular bone tissue can be further evaluated as a natural scaffold suitable for using in bone tissue engineering and restorative medicine.

Language:
Persian
Published:
Iranian Journal of Orthopaedic Surgery, Volume:19 Issue: 2, 2021
Pages:
83 to 90
https://magiran.com/p2398851  
دانلود و مطالعه متن این مقاله با یکی از روشهای زیر امکان پذیر است:
اشتراک شخصی
با عضویت و پرداخت آنلاین حق اشتراک یک‌ساله به مبلغ 1,390,000ريال می‌توانید 70 عنوان مطلب دانلود کنید!
اشتراک سازمانی
به کتابخانه دانشگاه یا محل کار خود پیشنهاد کنید تا اشتراک سازمانی این پایگاه را برای دسترسی نامحدود همه کاربران به متن مطالب تهیه نمایند!
توجه!
  • حق عضویت دریافتی صرف حمایت از نشریات عضو و نگهداری، تکمیل و توسعه مگیران می‌شود.
  • پرداخت حق اشتراک و دانلود مقالات اجازه بازنشر آن در سایر رسانه‌های چاپی و دیجیتال را به کاربر نمی‌دهد.
In order to view content subscription is required

Personal subscription
Subscribe magiran.com for 70 € euros via PayPal and download 70 articles during a year.
Organization subscription
Please contact us to subscribe your university or library for unlimited access!