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YY/T 1744-2020 English PDF

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YY/T 1744-2020: Tissue engineering medical device products - Bioactive ceramics - Method to measure cell migration in porous materials
Status: Valid
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YY/T 1744-2020299 Add to Cart 4 days Tissue engineering medical device products - Bioactive ceramics - Method to measure cell migration in porous materials Valid

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Basic data

Standard ID: YY/T 1744-2020 (YY/T1744-2020)
Description (Translated English): Tissue engineering medical device products - Bioactive ceramics - Method to measure cell migration in porous materials
Sector / Industry: Medical Device & Pharmaceutical Industry Standard (Recommended)
Classification of Chinese Standard: C35
Classification of International Standard: 11.040.30
Word Count Estimation: 16,128
Date of Issue: 2020-09-27
Date of Implementation: 2021-09-01
Regulation (derived from): Announcement No. 108 (2020) of the National Medical Products Administration
Issuing agency(ies): State Drug Administration

YY/T 1744-2020: Tissue engineering medical device products - Bioactive ceramics - Method to measure cell migration in porous materials


---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.
(Tissue engineering medical device products Bioactive ceramics Cell migration measurement methods in porous materials) ICS 11:040:30 C35 People's Republic of China Pharmaceutical Industry Standard Bioactive ceramics for tissue engineering medical device products Method for measuring cell migration in porous materials (ISO 19090:2018Tissue-engineeredmedicalproducts-Bioactive 2020-09-27 release 2021-09-01 implementation Issued by the State Drug Administration

Table of contents

Preface Ⅲ Introduction Ⅳ 1 Scope 1 2 Normative references 1 3 Terms and definitions 1 4 Principle 2 5 Test sample 2 6 Test Step 3 7 Calculation 9 8 Test report 10 Reference 12

Foreword

This standard was drafted in accordance with the rules given in GB/T 1:1-2009: This standard uses the redrafting method to modify and adopt ISO 19090:2018 ``Tissue Engineering Medical Products Bioactive Ceramic Porous Materials Method for measuring cell migration in the middle of the world: The technical differences between this standard and ISO 19090:2018 and the reasons are as follows: --- Regarding normative reference documents, this standard has made adjustments with technical differences to adapt to my country's technical conditions and adjustments: The situation is reflected in Chapter 2 "Normative Reference Documents", and the specific adjustments are as follows: ● Replace ISO 10993-5 with GB/T 16886:5 which is equivalent to the international standard: This standard also made the following editorial changes: --- Deleted Appendix A (informative appendix) "Experimental results used to determine experimental conditions" of ISO 19090:2018; --- Deleted Appendix B (informative appendix) "International Comparison Cycle Test Results" of ISO 19090:2018: Please note that certain contents of this document may involve patents: The issuing agency of this document is not responsible for identifying these patents: This standard was proposed by the State Drug Administration: This standard is organized by the National Standardization Technical Committee for Surgical Implants and Orthopaedic Devices, and the Sub-Technical Committee for Medical Device Products (SAC/TC110/SC3) Centralized: Drafting organizations of this standard: Sichuan University (Sichuan Medical Device Biological Materials and Products Inspection Center), China Food and Drug Control Research Institute: The main drafters of this standard: Liang Jie, Wei Lina, Yang Xiaoqin, Cai Yongfu, Yuan Tun, Zhang Le, Xu Liming:

Introduction

Bioactive ceramics are widely used in orthopedics and dentistry because of their good bioactivity and biocompatibility: And porous Bioactive ceramics, cells can enter the pores from the tissues, thus having the potential to effectively repair bone defects, and become a bone tissue engineering medical product: One of the potential candidate "raw materials" for cell scaffolds: In order to prove the clinical safety and effectiveness of bioactive ceramics, its physical, chemical and biological properties must first be tested: At the place Among the methods used, animal testing is the most important and necessary method to detect the biological characteristics of bioactive ceramics; however, in the 3R principle (instead of Substitute replacement, reduce reduction, optimize refinement), the number of animals and animal experiments must be reduced: Cell migration ability is the first and most important property of porous biomaterials (including bioactive ceramics): In porous biomaterials and their In the surrounding environment, if there is no cell migration, cell proliferation, differentiation, tissue formation and tissue maturation will not occur: There are currently two cell seeding methods used to test cell migration ability: one is to drop the cell suspension onto the surface of the porous material: The penetration ability of the cell suspension under the action of gravity was tested; the other is to add porous materials to the cell suspension to drive the cells into Into the material: These two methods can only detect the penetration and retention ability of cells, but they cannot simulate cell migration in the body: body fluid It is sufficient by itself to carry cells through the small gap between the implant material and the host bone tissue: Therefore, there is currently no simulation of cell behavior in vivo The report of the cell migration test method: When the porous bioceramic is implanted in the bone defect, the cells migrate into the hole to form new bone: In this process, the migration of osteoblasts Play an important role in bone conduction: In other words, without osteoblast migration, there will be no bone conduction or bone formation: Therefore, it is necessary to establish a method that can quantify and simulate the behavior of cells in the body to measure the cell migration potential of porous bioactive ceramics: Yes, in order to objectively evaluate its potential as a scaffold material for tissue engineering medical products: The standard drafting group adopted the following four materials: HT (HA: β-TCP=8: 2, average pore size 312:3μm, porosity 80:9%, pore structure is disordered, spherical), HTL (HA: β-TCP=6: 4, average pore size 390:3μm, porosity 81:7%, pore structure Disordered, spherical), TH (HA: β-TCP=1: 9, average pore size 375:4μm, porosity 81:6%, pore structure is disordered, spherical), THL (HA: β-TCP=3: 7, average pore diameter 293:8μm, porosity 77:7%, pore structure is disordered, spherical), which verifies this standard The method given in is feasible and operable for evaluating the cell migration potential of porous bioceramics: Bioactive ceramics for tissue engineering medical device products Method for measuring cell migration in porous materials

1 Scope

This standard specifies test methods for measuring and recording cell migration in porous bioactive ceramic materials: This standard applies to porous bioactive ceramics: This standard does not apply to porous materials with low or no cell adhesion, such as synthetic polymers and metals:

2 Normative references

The following documents are indispensable for the application of this document: For dated reference documents, only the dated version applies to this article Pieces: For undated references, the latest version (including all amendments) applies to this document: GB/T 16886:5 Biological evaluation of medical devices Part 5: In vitro cytotoxicity test (GB/T 16886:5-2017, ISO 10993-5:2009, IDT)

3 Terms and definitions

The following terms and definitions apply to this document: 3:1 Bioceramics Ceramic materials implanted in the human body to enhance biological functions: 3:2 Bioactive ceramics A bioceramic with guiding osseointegration performance when implanted in a bone defect: 3:3 Biomaterials Materials used for diagnosis, treatment, repair or replacement of body tissues and organs or to enhance their functions: [YY/T 1445-2016, definition 3:19] 3:4 Fulconfluent The monolayer of cells almost completely (≈95%~100%) covers the cell culture dish: 3:5 Complete medium Cell culture medium containing all necessary additives for the selected cell type: The cell culture medium has been verified by users It is beneficial and does not cause cell mutations: 3:6 Osteoblast-likecel An established cell line that is widely recognized as having "osteogenic activity":
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