1.Research Status of the Skeletalre Construction of Chest Wall.
Daixing ZHONG ; Lei WANG ; Xiaofei LI ; Lijun HUANG
Chinese Journal of Lung Cancer 2018;21(4):273-276
Chest wall defect may be caused by many factors such as the resection of tumor and trauma, and the reconstruction of bone-defection is still the key point of thoracic surgery. With the development of material science, more and more new materials have been used in medical practice, which makes huge progress in the surgery of chest wall. However, none of these materials satisfy all the practical needs of the reconstruction. Recently, with the development of the capacity of computer, 3D-printing technology has been gradually used in clinical work, and the idea of individual treatment has been accepted by more and more people. The weakness of these materials may be solved by the new material and the application of individual treatment, which could also make great advance in chest wall surgery. This article will make a summary of the research on the reconstruction of chest wall.
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Animals
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Biocompatible Materials
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chemical synthesis
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chemistry
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Humans
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Printing, Three-Dimensional
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Reconstructive Surgical Procedures
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instrumentation
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methods
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Thoracic Neoplasms
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surgery
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Thoracic Wall
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surgery
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transplantation
2.Study on the acid hydrolysis, fiber remodeling and bionics mineralization of rat tail tendon collagen type Ⅰ.
Zhan ZHANG ; Chun ZHANG ; Qiaofeng GUO
Journal of Zhejiang University. Medical sciences 2016;45(6):592-597
To produce bionic bone material that is consistent with human bone in chemical composition and molecular structure using rat tail tendon collagen type Ⅰ.The type Ⅰcollagen derived from rat tail was extracted by acetic acid to form collagen fibers. The reconstructed collagen fibers were placed in the mineralized solution to mimic bone mineralization for 2-6 days. Bone mineralization was observed by transmission electron microscopy and electron diffraction.Collagen fibers with characteristic D-Band structure were reconstructed by using rat tail tendon collagen type Ⅰ extracted with acid hydrolysis method. Transmission electron microscopy and electron diffraction showed that calcium hydroxyapatite precursor infiltrated into the collagen fibers, and the collagen fibers were partially mineralized after 2 days of mineralization; the collagen fibers were completely mineralized and bionic bone material of typeⅠ collagen/calcium hydroxyapatite was formed after 6 days of mineralization.The collagen type Ⅰ can be extracted from rat tail tendon by acid hydrolysis method, and can be reformed and mineralized to form the bionic bone material which mimics human bone in chemical composition and the molecular structure.
Animals
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Biocompatible Materials
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chemical synthesis
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Bone Matrix
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chemistry
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growth & development
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Bone Substitutes
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chemical synthesis
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Bone and Bones
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anatomy & histology
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chemistry
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Calcification, Physiologic
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Collagen Type I
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biosynthesis
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chemistry
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ultrastructure
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Humans
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Hydroxyapatites
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chemistry
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Rats
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Tail
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Tendons
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chemistry
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ultrastructure
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Tissue Engineering
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methods
3.Study of the preparation of silk fibroin gel and its morphology as drug release matrix in vitro and in vivo.
Qing LI ; Jie HUANG ; Fei HE ; Qingmei HE ; Chuanbao CAO ; Song WANG
Journal of Biomedical Engineering 2013;30(4):794-811
Silk fibroin (SF)/sodium alginate (SA) hydrogels can be used as drug injection materials. Homogenate was prepared by centrifugation of the pig myocardial extracellular matrix (PMM) and its modification of SF gel material. This paper observes and compares the different components SF, SF/SA, SF/SA/PMM to illustrate the SF/SA/PMM ternary material as a drug delivery composition material. This ternary material can shorten the gel time, and can make the gel form to be maintained better. Meanwhile, it makes the internal structure of the gel looser so that the hole wall becomes thinner and more conducive to the drug release. In addition, it has good biocompatibility proved by pathological analysis, and is able to enhance the mesenchymal stem cells growth activity, which has great significance in carrying out drug control release.
Alginates
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chemical synthesis
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chemistry
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Animals
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Biocompatible Materials
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chemical synthesis
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Delayed-Action Preparations
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chemistry
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Drug Carriers
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chemical synthesis
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chemistry
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Extracellular Matrix
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chemistry
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Fibroins
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chemical synthesis
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chemistry
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Glucuronic Acid
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chemical synthesis
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chemistry
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Hexuronic Acids
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chemical synthesis
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chemistry
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Hydrogels
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chemical synthesis
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chemistry
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Myocardium
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chemistry
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Rats
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Swine
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Tissue Extracts
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chemistry
4.Preparation of chitosan scaffold with different deacetylated degrees and evaluation of the degradation characteristics.
Minjian XIONG ; Xiaofeng LI ; Yan MIN ; Xiaoli XU ; Wenzhao CHEN ; Shanhu HUANG
Journal of Biomedical Engineering 2012;29(1):107-111
The chitosan scaffolds with different deacetylated degree were prepared in this study. The morphology of scaffolds were observed using SEM, and the porosity, the water absorbing swelling ratio and the degradation were examined both in vitro and in vitro. The results showed that the chitosan scaffolds with different deacetylated degree exhibited three-dimensional structure with high porosity. With increasing of deacetylated degree, their porosities were 93.46%, 90.02% and 86.71%, respectively. The swelling ratios of chitosan scaffolds were 820%, 803% and 772%, respectively. At the fourth week, the degradation rates were 30.44%, 22.08% and 17.10% in vitro, respectively; while the corresponding rates were 57.48%, 40.23%, 29.53% in vivo respectively. The degradation rate of chitosan scaffold was negatively correlated to deacetylated degree. Furthermore, it showed that the speed of degradation in vivo was faster than that in vitro. We concluded that controlling the deacetylated degree of chitosan can provide a well-matched degradable scaffold material for the reparation of cartilage defects.
Absorbable Implants
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Acetylation
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Animals
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Biocompatible Materials
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Chitosan
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analogs & derivatives
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chemical synthesis
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chemistry
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Female
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Male
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Materials Testing
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Rats
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Rats, Sprague-Dawley
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Tissue Engineering
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Tissue Scaffolds
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chemistry
5.Synthesis and characterization of N-octyl-N-arginine chitosan--a chitosan derivant with a mimetic structure of cell-penetrating peptides.
Chun-Yan LIU ; Rui-Rui PAN ; Tian-Yue JIANG ; Jian-Ping ZHOU ; Hui-Xia LÜ
Acta Pharmaceutica Sinica 2012;47(6):797-802
A novel chitosan derivant, N-octyl-N-arginine chitosan (OACS) with a mimetic structure of cell-penetrating peptides was synthesized by introducing hydrophilic arginine groups and hydrophobic octyl groups to the amino-group on chitosan's side chain. Structure of the obtained polymer was characterized by FT-IR and 1H NMR. The substitution degree of octyl and arginine groups was calculated through element analysis and spectrophotometric method, separately. The critical micelle concentration of OACS was 0.12 - 0.27 mgmL(-1) tested by fluorescence spectrometry. The solubility test showed OACS could easily dissolve in pH 1 - 12 solutions and self-assemble to form a micelle solution with light blue opalescence. The OACS micelles have a mean size of 158.4 - 224.6 nm, polydisperse index of 0.038 - 0.309 and a zeta potential of +19.16 - +30.80 mV determined by malvern zetasizer. AFM images confirmed free OACS micelle has a regular sphere form with a uniform particle size. MTT test confirmed that OACS was safe in 50 - 1 000 micromol-L(-1). The result of HepG2 cell experiment showed that the cell internalization of OACS micelles enhanced with increased substitution degree of arginine by 40 folds compared to chitosan. Thus, OACS micelles were a promising nano vehicle with permeation enhancement and drug carrier capability.
Arginine
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analogs & derivatives
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chemical synthesis
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chemistry
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metabolism
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Biocompatible Materials
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chemical synthesis
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chemistry
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Cell Survival
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Cell-Penetrating Peptides
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chemical synthesis
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chemistry
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Chitosan
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analogs & derivatives
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chemical synthesis
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chemistry
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Drug Carriers
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Hep G2 Cells
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Humans
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Magnetic Resonance Spectroscopy
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Micelles
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Nanoparticles
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Particle Size
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Polymers
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Solubility
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Spectroscopy, Fourier Transform Infrared
6.Preparation of alpha-tricalcium phosphate/HA whisker/carboxymethyl chitosan-gelatin composite porous bone cement.
Dongjuan WEI ; Xiang ZHANG ; Jianwen GU ; Ping HU ; Weizhong YANG ; Dongning CHEN ; Dali ZHOU
Journal of Biomedical Engineering 2012;29(3):491-495
In order to investigate the effects of HA whisker and carboxymethyl chitosan-gelatin(CMC-Gel) on the mechanical properties of porous calcium phosphate cement, a series of alpha-tricalcium phosphate (alpha-TCP), HA whisker and L-sodium glutamate porogen with different mass fractions were mixed, and setting liquid was added to them to prepare alpha-TCP/HA whisker composite porous bone cement. Then, the cement was immersed in a series of CMC-Gel solutions which had different weight ratios of CMC to Gel to prepare alpha-TCP/HA whisker/CMC-Gel composite porous bone cement. The compressive strengths and microstructure of cement were characterized by mechanical testing machine and SEM. The results showed that when the mass fraction of HA whisker is 4%, the compressive strength of alpha-TCP/HA whisker composite porous bone cement reaches 2.57MPa, which is 1.81 times that of alpha-TCP bone cement. When the weight ratio of CMC to Gel is 50:50, the compressive strength of alpha-TCP/HA whisker/CMC-Gel composite porous bone cement is 3. 34MPa, which is 2.35 times that of alpha-TCP bone cement, and the toughness of the composite cement is greatly improved as well.
Biocompatible Materials
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chemistry
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pharmacology
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Bone Cements
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chemical synthesis
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Calcium Phosphates
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chemistry
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Chitosan
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analogs & derivatives
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chemical synthesis
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chemistry
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Compressive Strength
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Gelatin
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chemistry
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Hydroxyapatites
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chemical synthesis
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chemistry
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Porosity
7.Study on preparation and physicochemical properties of surface modified sintered bone.
Jingfeng LI ; Qixin ZHENG ; Xiaodong GUO
Journal of Biomedical Engineering 2012;29(3):474-478
The aim of this study is to investigate a new method for preparing a biomimetic bone material-surface modified sintered bovine cancellous bone, and to improve its bioactivity as a tissue engineering bone. The prepared sintered bovine cancellous bones with the same size were randomly divided into two groups, immersing in 1 and 1. 5 times simulated body fluid (SBF), respectively. The three time periods of soak time were 7, 14, and 21 days. After sintered bone was dried, the surface morphology of sintered bone and surface mineralization composition were observed under scanning electron microscopy (SEM). By comparing the effect of surface modification of sintered bone materials, we chose the most ideal material and studied its pore size, the rate of the porosity, the compress and bend intensity. And then the material and the sintered bone material without surface modification were compared. The study indicated that sintered bone material immersed in SBF (1.5 times) for 14 days showed the best effect of surface modification, retaining the original physico-chemical properties of sintered bone.
Animals
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Biocompatible Materials
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chemical synthesis
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Biomimetic Materials
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chemical synthesis
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Bone Substitutes
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Bone and Bones
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chemistry
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drug effects
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Calcification, Physiologic
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physiology
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Cattle
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Chemical Phenomena
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Hydroxyapatites
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chemistry
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Porosity
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Surface Properties
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Tissue Engineering
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methods
8.In vitro biologic evaluation on nano-hydroxyapatite/poly (L-lactic acid) biocomposites fabricated using in-situ growth method.
Caiyun ZHANG ; Qianfeng FENG ; Tao ZHANG ; Jin CHEN ; Chuanhua LU ; Hongfei WU
Journal of Biomedical Engineering 2012;29(2):307-310
The aim of this research was to estimate the bioactivity of nano-hydroxyapatite/poly (L-lactic acid) composites in simulated body fluid. In vitro test showed that the pH value of simulated body fluid (SBF) declined gradually and the existence of hydroxyapatite (HA) particles neutralized the acid degradation product of poly (L-lactic acid) (PLLA). Bone-like apatite deposited on the surface, and silkworm-like crystals and plate-like clusters appeared after soaking. At the same time, there were many honeycomb-like pores caused by nano-composite degraded. The results indicated that the hydroxyapatite/poly (L-lactic acid) nano-composites have good bioactivity and degradation characteristics.
Biocompatible Materials
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Bone Substitutes
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chemical synthesis
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chemistry
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Durapatite
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chemical synthesis
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chemistry
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Lactic Acid
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chemistry
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Microscopy, Electron, Scanning
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Nanoparticles
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Polyesters
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chemical synthesis
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chemistry
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Polymers
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chemistry
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Porosity
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X-Ray Diffraction
9.Biocompatibility of alpha-calcium sulfate hemihydrate (CSH)/multi-walled carbon nanotube (MWCNT) composites for bone reconstruction application.
Yi LOU ; Zongyou PAN ; Ruikai WU ; Enxing XUE ; Libo JIANG ; Guangyong YANG ; Yang ZHOU ; Jianli LIU ; Qing HUANG ; Huazi XU
Chinese Journal of Biotechnology 2012;28(3):340-348
We examined the biocompatibility and the safety of a-calcium sulfate hemihydrate (CSH)/multi-walled carbon nanotube (MWCNT) composites for bone reconstruction application. The biocompatibility of the CSH/MWCNT composites was evaluated by the measures which taking L929 fibroblast cells cultured in the extracted liquid of the composite soaking solution and putting bone marrow stromal cells planted on the composite pellets in vitro, respectively. The cell proliferation was evaluated by MTT test and further observed using an inverted optical microscope and a scanning electric microscope. The toxicity of the composites was evaluated by acute and subacute systemic toxicity test. Long-term muscle and bone implantation in vivo tests were also conducted. L929 fibroblast cells grew well in the extracted liquid, as well as bone marrow stromal cells that could adhere on the surface of sample pellets and proliferated rapidly. MTT test showed that there were no significant differences between the experimental and control groups (P > 0.05). In vivo test manifested that the composites were no toxicity, no irritation to skin and good for bone defect reconstruction. It was proved that a-calcium sulfate hemihydrate (CSH)/multi-walled carbon nanotube (MWCNT) composites exhibited excellent biocompatibility for the potential application in bone tissue engineering.
Animals
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Biocompatible Materials
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chemistry
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Bone Marrow Cells
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cytology
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Bone Substitutes
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chemical synthesis
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chemistry
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Calcium Sulfate
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chemistry
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Cell Line
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Cell Proliferation
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Fibroblasts
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cytology
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Materials Testing
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Nanotubes, Carbon
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chemistry
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Rabbits
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Stromal Cells
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cytology
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Tissue Engineering
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methods
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Toxicity Tests
10.Advancement of research on polyamidoamine dendrimers.
Journal of Biomedical Engineering 2012;29(5):1003-1006
Polyamidoamine (PAMAM) dendrimers is synthesized by the American scientist, Tomalia, in 1985 and is now used widely in many fields such as gene carriers, photoelectric sensor, wastewater treatment, drug carriers and catalyst. The present paper mainly reviews the structure and methods of synthesis, celluar cytotoxicity, achievements of gene and drug carriers research, advancement and prospect of PAMAM as a carrier in glioma therapy. Besides, it also involves an outline for the future research of the radiotherapy for glioma.
Biocompatible Materials
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chemical synthesis
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chemistry
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Dendrimers
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chemical synthesis
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chemistry
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Drug Carriers
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Genetic Vectors

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