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1.
Int J Nanomedicine ; 14: 8603-8610, 2019.
Article in English | MEDLINE | ID: mdl-31802872

ABSTRACT

PURPOSE: The primary goal of the present study was to develop the nano-drug consisting of doxorubicin and exosome derived from mesenchymal stem cells, and to explore its effect on osteosarcoma in vitro. METHODS: The exosomes were isolated from bone marrow MSCs (BM-MSCs) by an Exosome Isolation Kit. The exosome-loaded doxorubicin (Exo-Dox) was prepared by mixing exosome with Dox-HCl, desalinizing with triethylamine and then dialyzing against PBS overnight. The nanoparticle tracking analysis (NTA) and transmission electron microscope (TEM) were used to characterize of the exosome and Exo-Dox. The cytotoxicity of Exo-Dox was determined by CCK-8 assay. Further, the cellular uptake of different drugs was analyzed using inverted fluorescence microscope and flow cytometry. RESULTS: The typical exosome structures can be observed by TEM. After loading with doxorubicin, its size is larger than free exosome. Compared with the free Dox, the prepared Exo-Dox showed enhanced cellular uptake efficiency and anti-tumor effect in osteosarcoma MG63 cell line but low cytotoxicity in myocardial H9C2 cell line. CONCLUSION: The prepared Exo-Dox could be used as an excellent chemotherapeutic drug for treatment of osteosarcoma in vitro. Considering the tumor-homing feature of BM-MSCs, the Exo-Dox may be a good candidate for targeted osteosarcoma treatment in future study.


Subject(s)
Doxorubicin/therapeutic use , Exosomes/metabolism , Mesenchymal Stem Cells/metabolism , Nanoparticles/chemistry , Osteosarcoma/drug therapy , Animals , Antineoplastic Agents/pharmacology , Antineoplastic Agents/therapeutic use , Bone Neoplasms/drug therapy , Bone Neoplasms/pathology , Cell Death/drug effects , Cell Line, Tumor , Cell Survival/drug effects , Doxorubicin/pharmacology , Drug Liberation , Exosomes/ultrastructure , Humans , Mice , Nanoparticles/ultrastructure , Osteosarcoma/pathology , Rats
2.
Int J Nanomedicine ; 10: 2219-28, 2015.
Article in English | MEDLINE | ID: mdl-25834434

ABSTRACT

A sensitive electrochemical immunosensor was developed for detection of alpha-fetoprotein (AFP) based on a three-dimensional nanostructure gold electrode using a facile, rapid, "green" square-wave oxidation-reduction cycle technique. The resulting three-dimensional gold nanocomposites were characterized by scanning electron microscopy and cyclic voltammetry. A "sandwich-type" detection strategy using an electrochemical immunosensor was employed. Under optimal conditions, a good linear relationship between the current response signal and the AFP concentrations was observed in the range of 10-50 ng/mL with a detection limit of 3 pg/mL. This new immunosensor showed a fast amperometric response and high sensitivity and selectivity. It was successfully used to determine AFP in a human serum sample with a relative standard deviation of <5% (n=5). The proposed immunosensor represents a significant step toward practical application in clinical diagnosis and monitoring of prognosis.


Subject(s)
Biosensing Techniques/instrumentation , Electrochemical Techniques/instrumentation , Electrodes , Nanocomposites/chemistry , Antibodies/chemistry , Biosensing Techniques/methods , Equipment Design , Gold/chemistry , Humans , Limit of Detection , Microscopy, Electron, Scanning , Reproducibility of Results , Sensitivity and Specificity , alpha-Fetoproteins/analysis , alpha-Fetoproteins/immunology
3.
Talanta ; 125: 439-45, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24840469

ABSTRACT

A facile electrochemical immunosensor based on graphene-three dimensional nanostructure gold nanocomposites (G-3D Au) using simple and rapid one-step electrochemical co-reduction technique was developed for sensitive detection of topoisomerase. The resultant G-3D Au nanocomposites were characterized by scanning electron microscopy, cyclic voltammetry and electrochemical impedance spectroscopy, and then were used as a substrate for construction of the "sandwich-type" immunosensor. Amperometric current-time curve was employed to monitor the immunoreaction on the protein modified electrode. The proposed method could respond to topoisomerase with a linear calibration range from 0.5 ng mL(-1) to 50 ng mL(-1) with a detection limit of 10 pg mL(-1). This new biosensor exhibited a fast amperometric response, high sensitivity and selectivity, and was successfully used in determining the topoisomerase which was added in human serum with a relative standard deviation (n=5)<5%. The immunosensor served as a significant step toward the practical application of the immunosensor in clinical diagnosis and prognosis monitor.


Subject(s)
Biosensing Techniques , DNA Topoisomerases, Type I/analysis , Electrochemistry/instrumentation , Gold/chemistry , Graphite/chemistry , Metal Nanoparticles/chemistry , Nanocomposites/chemistry , DNA Topoisomerases, Type I/blood , Electrodes , Enzyme-Linked Immunosorbent Assay , Humans , Microscopy, Electron, Scanning , Nanotechnology , Neoplasms/diagnosis , Reproducibility of Results
4.
Microsurgery ; 33(8): 638-45, 2013 Nov.
Article in English | MEDLINE | ID: mdl-24105647

ABSTRACT

BACKGROUND: Defects sustained at the distal forearm are common and pedicled perforator flaps have unique advantages in resurfacing it. The purpose of this study is to reappraise the anatomy of the perforator in the posterolateral aspect of the mid-forearm and present our clinical experience on using perforator flaps based on it for reconstruction of defects in the distal forearm. METHODS: This study was divided into anatomical study and clinical application. In the anatomical study, 30 preserved upper limbs were used. Clinically, 11 patients with defects at the forearm underwent reconstruction with the posterolateral mid-forearm perforator flaps. The defects, ranging from 4.5 × 2.5 cm to 10.5 × 4.5 cm, were located at the dorsal aspect of the distal forearm in 6 cases and at the volar aspect of the distal forearm in 5 cases. RESULTS: Three patterns of the perforator were observed in the posterolateral aspect of the mid-forearm, which originated from the posterior interosseous artery, the proximal segment of the radial artery or the radial recurrent artery, and the middle segment of the radial artery, respectively. The perforator was located 11.8 ± 0.2 cm to 15.8 ± 0.4 cm inferior to the lateral humeral epicondyle. Clinically, flaps in 8 cases survived uneventfully, while the other 3 cases suffered mild marginal epidermal necrosis, which was cured with continuous dress changing. CONCLUSION: The location of the perforator at the posterolateral aspect of the mid-forearm is consistent; the posterolateral mid-forearm perforator flap is particularly suitable to cover defects in the distal one-third of the forearm.


Subject(s)
Forearm Injuries/surgery , Forearm/blood supply , Perforator Flap/blood supply , Plastic Surgery Procedures/methods , Soft Tissue Injuries/surgery , Adult , Aged , Female , Forearm/surgery , Humans , Male , Middle Aged , Radial Artery/anatomy & histology , Radial Artery/surgery , Treatment Outcome
5.
Anal Chim Acta ; 767: 50-8, 2013 Mar 12.
Article in English | MEDLINE | ID: mdl-23452786

ABSTRACT

A novel electrochemical DNA biosensor based on graphene-three dimensional nanostructure gold nanocomposite modified glassy carbon electrode (G-3D Au/GCE) was fabricated for detection of survivin gene which was correlated with osteosarcoma. The G-3D Au film was prepared with one-step electrochemical coreduction with graphite oxide and HAuCl4 at cathodic potentials. The active surface area of G-3D Au/GCE was 2.629cm(2), which was about 3.8 times compared to that of a Au-coated GCE under the same experimental conditions, and 8.8 times compared to a planar gold electrode with a similar geometric area. The resultant nanocomposites with high conductivity, electrocatalysis and biocompatibility were characterized by scanning electron microscopy (SEM), cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). A "sandwich-type" detection strategy was employed in this electrochemical DNA biosensor and the response of this DNA biosensor was measured by CV and amperometric current-time curve detection. Under optimum conditions, there was a good linear relationship between the current signal and the logarithmic function of complementary DNA concentration in a range of 50-5000fM with a detection limit of 3.4fM. This new biosensor exhibited a fast amperometric response, high sensitivity and selectivity and has been used in a polymerase chain reaction assay of real-life sample with a satisfactory result.


Subject(s)
Biosensing Techniques , DNA/analysis , Electrochemical Techniques , Gold/chemistry , Graphite/chemistry , Metal Nanoparticles/chemistry , Osteosarcoma/genetics , Electrodes , Microscopy, Electron, Scanning , Oxidation-Reduction , Oxides/chemistry
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