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Synergistic intrafibrillar/extrafibrillar mineralization of collagen scaffolds based on a biomimetic strategy to promote the regeneration of bone defects.基于仿生策略的胶原蛋白支架协同纤维内/纤维外矿化以促进骨缺损再生
Int J Nanomedicine. 2016 May 12;11:2053-67. doi: 10.2147/IJN.S102844. eCollection 2016.
2
[EFFECTIVENESS COMPARISON OF USING BONE TRANSPORT AND BONE SHORTENING-LENGTHENING FOR TIBIAL BONE AND SOFT TISSUE DEFECTS].[骨搬运与骨缩短延长术治疗胫骨骨与软组织缺损的疗效比较]
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2014 Jul;28(7):818-22.
3
Kidney-targeted transplantation of mesenchymal stem cells by ultrasound-targeted microbubble destruction promotes kidney repair in diabetic nephropathy rats.超声靶向微泡破坏介导间充质干细胞肾靶向移植促进糖尿病肾病大鼠肾脏修复。
Biomed Res Int. 2013;2013:526367. doi: 10.1155/2013/526367. Epub 2013 May 27.
4
New development and application of ultrasound targeted microbubble destruction in gene therapy and drug delivery.超声靶向微泡破坏在基因治疗和药物传递中的新发展和应用。
Curr Gene Ther. 2013 Aug;13(4):250-74. doi: 10.2174/15665232113139990003.
5
Selective laser melting-produced porous titanium scaffolds regenerate bone in critical size cortical bone defects.选择性激光熔化制备的多孔钛支架可在临界尺寸皮质骨缺损中再生骨。
J Orthop Res. 2013 May;31(5):792-9. doi: 10.1002/jor.22293. Epub 2012 Dec 19.
6
Treatment of posttraumatic bone defects by the induced membrane technique.诱导膜技术治疗外伤性骨缺损。
Orthop Traumatol Surg Res. 2012 Feb;98(1):97-102. doi: 10.1016/j.otsr.2011.11.001. Epub 2012 Jan 12.
7
Ultrasound-targeted microbubble destruction enhances naked plasmid DNA transfection in rabbit Achilles tendons in vivo.超声靶向破坏微泡增强体内兔跟腱中裸露质粒 DNA 的转染。
Gene Ther. 2012 Jul;19(7):703-10. doi: 10.1038/gt.2011.165. Epub 2011 Oct 27.
8
Ultrasound and microbubble-assisted gene delivery in Achilles tendons: long lasting gene expression and restoration of fibromodulin KO phenotype.超声联合微泡辅助基因转染修复跟腱:长期的基因表达和纤维调节素 KO 表型的恢复。
J Control Release. 2011 Dec 10;156(2):223-30. doi: 10.1016/j.jconrel.2011.08.020. Epub 2011 Aug 23.
9
Explorations of high-intensity therapeutic ultrasound and microbubble-mediated gene delivery in mouse liver.高强度治疗超声和微泡介导的基因传递在小鼠肝脏中的探索。
Gene Ther. 2011 Oct;18(10):1006-14. doi: 10.1038/gt.2011.34. Epub 2011 Mar 31.
10
Repeated and targeted transfer of angiogenic plasmids into the infarcted rat heart via ultrasound targeted microbubble destruction enhances cardiac repair.经超声靶向微泡破坏将血管生成质粒反复、靶向递送至梗死大鼠心脏可增强心脏修复。
Eur Heart J. 2011 Aug;32(16):2075-84. doi: 10.1093/eurheartj/ehq475. Epub 2010 Dec 31.

超声介导微泡破坏增强绿色荧光蛋白基因转染在骨缺损中的研究

[Research of enhanced green fluorescent protein gene transfer with ultrasound-mediated microbubble destruction in bone defects].

作者信息

Li Shiwei, Xie Xiaoli, Yang Xiaodong, Liu Lijun, Tang Xueyang

机构信息

Department of Pediatric Surgery, West China Hospital, Sichuan University, Chengdu Sichuan, 610041, P.R.China.

Department of Pediatric Surgery, Guangzhou Women and Children's Medical Center, Guangzhou Guangdong, 510623, P.R.China.

出版信息

Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2017 Apr 15;31(4):437-442. doi: 10.7507/1002-1892.201611059.

DOI:10.7507/1002-1892.201611059
PMID:29798609
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8498166/
Abstract

OBJECTIVE

To investigate the effect of ultrasonic irradiation time on enhanced green fluorescent protein (EGFP) gene transfection efficiency and local tissue in bone defects using ultrasound-mediated microbubble destruction.

METHODS

Thirty 3-month-old New Zealand rabbits (2.5-3.0 kg in weight) were randomly divided into 5 groups ( =6) and bone defect models were made on the right ulna. At 10 days after modeling, suspension of microbubbles and EGFP plasmids were locally injected (0.3 mL/kg) and then ultrasound was performed on defect at a frequency of 1 MHz, a intensity of 0.5 W/cm , and a duty ratio of 20% for 1, 2, 3, 4, and 5 minutes respectively (in 1, 2, 3, 4, and 5 minutes groups respectively). The survival condition was observed. Rabbits were sacrificed for gross observation at 7 days after transfer. The gene expression was observed by fluorescence staining. HE staining and transmission electron microscopy were used to observe the local tissue damage.

RESULTS

The animals all survived. New soft tissue formed in bone defects area at 1 week after transfer, the surrounding muscle tissue was partly filled in it. Green fluorescence expression was observed in all rabbits. The expression was the strongest in 2 minutes group, and was the weakest in 1 minute group. The absorbance ( ) value showed significant differences when compared 1 minute and 2 minutes groups with other groups ( <0.05), but no significant difference was found between 3, 4, and 5 minutes groups ( >0.05). Tissue damage was observed in all groups and it was aggravated with the increase of irradiation time.

CONCLUSION

EGFP transfection efficiency in bone defect by ultrasound-mediated microbubble destruction is related to irradiation time. EGFP gene can be efficiently transfected without obvious toxicity at 1 MHz, 0.5W/cm , and duty ratio of 20% for 2 minutes in bone defects of rabbits.

摘要

目的

探讨超声辐照时间对超声介导微泡破坏增强绿色荧光蛋白(EGFP)基因转染效率及骨缺损局部组织的影响。

方法

将30只3月龄新西兰兔(体重2.5 - 3.0 kg)随机分为5组(每组n = 6),于右侧尺骨制作骨缺损模型。造模后10天,局部注射微泡与EGFP质粒混悬液(0.3 mL/kg),然后分别以1 MHz频率、0.5 W/cm²强度、20%占空比,对缺损部位进行1、2、3、4、5分钟超声辐照(分别为1、2、3、4、5分钟组)。观察动物存活情况。转染后7天处死兔子进行大体观察。通过荧光染色观察基因表达情况。采用苏木精-伊红(HE)染色及透射电子显微镜观察局部组织损伤情况。

结果

动物均存活。转染后1周骨缺损区有新的软组织形成,周围肌肉组织部分填充其中。所有兔子均观察到绿色荧光表达。2分钟组表达最强,1分钟组最弱。1分钟组和2分钟组与其他组比较吸光度(A)值差异有统计学意义(P < 0.05),但3、4、5分钟组之间差异无统计学意义(P > 0.05)。所有组均观察到组织损伤,且随辐照时间延长而加重。

结论

超声介导微泡破坏在骨缺损中EGFP转染效率与辐照时间有关。在兔骨缺损中,以1 MHz频率、0.5W/cm²强度、20%占空比超声辐照2分钟可有效转染EGFP基因且无明显毒性。