Jinsong Ren
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Jinsong Ren has a total of 62 co-authors. Here are the top co-authors by number of shared publications:
- Xiaogang Qu
Laboratory of Chemical Biology, Division of Biological Inorganic Chemistry, State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Graduate School of the Chinese Academy of Sciences, Chinese Academy of Sciences, Changchun, Jilin 130022, China
38 shared publications - Fang Pu
State Key Laboratory of Rare Earth Resource Utilization and Laboratory of Chemical Biology Changchun Institute of Applied Chemistry Chinese Academy of Sciences Changchun Jilin People's Republic of China
27 shared publications Xiaogang Qu
Laboratory of Chemical Biology and State Key laboratory of Rare Earth Resources Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, 130022 P.R. China
21 shared publications- Zhen Liu
Jilin Provincial Key Laboratory of Tooth Development and Bone Remodeling School and Hospital of Stomatology Jilin University Changchun 130021 China
17 shared publications - Zhenhua Li
The Tenth Affiliated Hospital, Southern Medical University (Dongguan People's Hospital), Dongguan, Guangdong, China.
15 shared publications - Xinjian Yang
College of Chemistry & Materials Science, State Key Laboratory of New Pharmaceutical Preparations and Excipients, Key Laboratory of Medicinal Chemistry and Molecular Diagnosis of the Ministry of Education, Chemical Biology Key Laboratory of Hebei Province, Hebei University, Baoding, 071002, PR China
14 shared publications
Latest Publications
- 1 February 2017
- Published by Elsevier in Analytica Chimica Acta
- Vol. 952, 88-95
Immobilization of enzyme on chiral polyelectrolyte surface
- 1 February 2017
- Published by Elsevier in Analytica Chimica Acta
- Vol. 952, 88-95
Immobilization of enzyme on chiral polyelectrolyte surface
- 1 October 2014
- Published by Elsevier in Biomaterials
- Vol. 35 (30) , 8694-8702
DNA-mediated biomineralization of rare-earth nanoparticles for simultaneous imaging and stimuli-responsive drug delivery
- 1 October 2014
- Published by Elsevier in Biomaterials
- Vol. 35 (30) , 8694-8702
DNA-mediated biomineralization of rare-earth nanoparticles for simultaneous imaging and stimuli-responsive drug delivery
- 22 November 2013
- Published by Royal Society of Chemistry (RSC) in Nanoscale
- Vol. 6 (4) , 2211-2217
Biocompatible and high-performance amino acids-capped MnWO4 nanocasting as a novel non-lanthanide contrast agent for X-ray computed tomography and T1-weighted magnetic resonance imaging
In the present work, a novel non-lanthanide dual-modality contrast agent, manganese tungstate (MnWO4), has been successfully constructed by a facile and versatile hydrothermal route. With the merits of a high atomic number and a well-positioned K-edge energy of tungsten, our well-prepared non-lanthanide nanoprobes provide a higher contrast efficacy than routine iodine-based agents in clinics. Additionally, the presence of Mn in these nanoparticles endow them with excellent T1-weighted MR imaging capabilities. As an alternative to T2-weighted MRI and CT dual-modality contrast agents, the nanoprobes can provide a positive contrast signal, which prevents confusion with the dark signals from hemorrhage and blood clots. To the best of our knowledge, this is the first report that a non-lanthanide imaging nanoprobe is applied for CT and T1-weighted MRI simultaneously. Moreover, comparing with gadolinium-based T1-weighted MRI and CT dual-modality contrast agents that were associated with nephrogenic systemic fibrosis (NSF), our contrast agents have superior biocompatibility, which is proved by a detailed study of the pharmacokinetics, biodistribution, and in vivo toxicology. Together with excellent dispersibility, high biocompatibility and superior contrast efficacy, these nanoprobes provide detailed and complementary information from dual-modality imaging over traditional single-mode imaging and bring more opportunities to the new generation of non-lanthanide nanoparticulate-based contrast agents.
- 22 November 2013
- Published by Royal Society of Chemistry (RSC) in Nanoscale
- Vol. 6 (4) , 2211-2217
Biocompatible and high-performance amino acids-capped MnWO4 nanocasting as a novel non-lanthanide contrast agent for X-ray computed tomography and T1-weighted magnetic resonance imaging
In the present work, a novel non-lanthanide dual-modality contrast agent, manganese tungstate (MnWO4), has been successfully constructed by a facile and versatile hydrothermal route. With the merits of a high atomic number and a well-positioned K-edge energy of tungsten, our well-prepared non-lanthanide nanoprobes provide a higher contrast efficacy than routine iodine-based agents in clinics. Additionally, the presence of Mn in these nanoparticles endow them with excellent T1-weighted MR imaging capabilities. As an alternative to T2-weighted MRI and CT dual-modality contrast agents, the nanoprobes can provide a positive contrast signal, which prevents confusion with the dark signals from hemorrhage and blood clots. To the best of our knowledge, this is the first report that a non-lanthanide imaging nanoprobe is applied for CT and T1-weighted MRI simultaneously. Moreover, comparing with gadolinium-based T1-weighted MRI and CT dual-modality contrast agents that were associated with nephrogenic systemic fibrosis (NSF), our contrast agents have superior biocompatibility, which is proved by a detailed study of the pharmacokinetics, biodistribution, and in vivo toxicology. Together with excellent dispersibility, high biocompatibility and superior contrast efficacy, these nanoprobes provide detailed and complementary information from dual-modality imaging over traditional single-mode imaging and bring more opportunities to the new generation of non-lanthanide nanoparticulate-based contrast agents.
- 22 October 2013
- Published by Wiley in Advanced Functional Materials
- Vol. 24 (4) , 522-529
A Multi‐synergistic Platform for Sequential Irradiation‐Activated High‐Performance Apoptotic Cancer Therapy
Artificial hyperthermia is an emerging technique to induce apoptotic cancer cell death. However, achieving effective hyperthermic apoptosis is often difficult, as cells typically acquire resistance to thermal stress. With the aid of sequential irradiation, highly integrated nanoassemblies based on reduced graphene oxide–ZnO nanoparticles–hyaluronic acid (rGo‐ZnO‐HA) can serve as a multi‐synergistic platform for targeted high‐performance apoptotic cancer therapy. The surface engineering of ZnO/graphene hybrid with multifunctional HA biomacromolecules simultaneously confers the system colloidal stability, biocompatibility, and a cancer cell targeting ability. After receptor‐mediated endocytosis, enzyme‐mediated fluorescence activation helps track cellular uptake and provides truly molecular imaging. Furthermore, the reactive oxygen species (ROS) generated by ZnO/rGo under light illumination can effectively sensitize cancer cells to the subsequent NIR laser‐induced apoptotic hyperthermia. In particular, photo modulation of cellular ROS to sensitize cells provides a novel approach to increase the efficacy of hyperthermic apoptosis. These findings suggest that a powerful apoptotic therapeutic platform could be achieved based on the multi‐synergistic platform.
- 22 October 2013
- Published by Wiley in Advanced Functional Materials
- Vol. 24 (4) , 522-529
A Multi‐synergistic Platform for Sequential Irradiation‐Activated High‐Performance Apoptotic Cancer Therapy
Artificial hyperthermia is an emerging technique to induce apoptotic cancer cell death. However, achieving effective hyperthermic apoptosis is often difficult, as cells typically acquire resistance to thermal stress. With the aid of sequential irradiation, highly integrated nanoassemblies based on reduced graphene oxide–ZnO nanoparticles–hyaluronic acid (rGo‐ZnO‐HA) can serve as a multi‐synergistic platform for targeted high‐performance apoptotic cancer therapy. The surface engineering of ZnO/graphene hybrid with multifunctional HA biomacromolecules simultaneously confers the system colloidal stability, biocompatibility, and a cancer cell targeting ability. After receptor‐mediated endocytosis, enzyme‐mediated fluorescence activation helps track cellular uptake and provides truly molecular imaging. Furthermore, the reactive oxygen species (ROS) generated by ZnO/rGo under light illumination can effectively sensitize cancer cells to the subsequent NIR laser‐induced apoptotic hyperthermia. In particular, photo modulation of cellular ROS to sensitize cells provides a novel approach to increase the efficacy of hyperthermic apoptosis. These findings suggest that a powerful apoptotic therapeutic platform could be achieved based on the multi‐synergistic platform.
- 20 September 2013
- Published by Wiley in Advanced Functional Materials
- Vol. 24 (7) , 1004-1010
Engineered CpG‐Antigen Conjugates Protected Gold Nanoclusters as Smart Self‐Vaccines for Enhanced Immune Response and Cell Imaging
A facile one‐pot synthesis of fluorescent AuNCs by using ovalbumin‐CpG oligodeoxynucleotides (ODNs) conjugates as the templates, which can elicit specific immunological responses, is demonstrated. Through dual‐delivery of protein antigen and CpG ODNs, the as‐prepared AuNCs can act as smart self‐vaccines to assist in generation of high immunostimulatory activity while simultaneously act as an imaging agent. The AuNCs‐based vaccines are not thought to have not been reported so far, making this platform the first example of the usage of AuNCs as effective vaccines. Furthermore, compared with the antigen, the immunostimulatory activity of the as‐prepared AuNCs can not only be retained, but also can be effectively enhanced. These findings suggest the AuNCs‐based vaccines may be utilized as safe and efficient immunostimulatory agents that are able to prevent and/or treat a variety of ailments.
- 20 September 2013
- Published by Wiley in Advanced Functional Materials
- Vol. 24 (7) , 1004-1010
Engineered CpG‐Antigen Conjugates Protected Gold Nanoclusters as Smart Self‐Vaccines for Enhanced Immune Response and Cell Imaging
A facile one‐pot synthesis of fluorescent AuNCs by using ovalbumin‐CpG oligodeoxynucleotides (ODNs) conjugates as the templates, which can elicit specific immunological responses, is demonstrated. Through dual‐delivery of protein antigen and CpG ODNs, the as‐prepared AuNCs can act as smart self‐vaccines to assist in generation of high immunostimulatory activity while simultaneously act as an imaging agent. The AuNCs‐based vaccines are not thought to have not been reported so far, making this platform the first example of the usage of AuNCs as effective vaccines. Furthermore, compared with the antigen, the immunostimulatory activity of the as‐prepared AuNCs can not only be retained, but also can be effectively enhanced. These findings suggest the AuNCs‐based vaccines may be utilized as safe and efficient immunostimulatory agents that are able to prevent and/or treat a variety of ailments.
- 23 August 2013
- Published by IOP Publishing in Nanotechnology
- Vol. 24 (37) , 375603
Lighting up silica nanotubes transcribed from the submicron structure of a metal–peptide hybrid
Fluorescent silica nanotubes are attracting increasing interest because of their versatile applicability in a range of diverse fields. By using sol-gel transcription of tetraethylorthosilicate (TEOS) from various soft templates, silica nanotubes can be conveniently prepared. Metal-peptide hybrids with well-defined nanostructures and outstanding functionalities are very interesting candidates to serve as templates. Herein, we demonstrate that glutathione (GSH) can act as a building block for a bioinspired structure with dimensions down to the nanoscale, based on specific interactions between metal ions and the peptide. Congo red is able to selectively stain the nanofibres obtained, and appears apple-green in colour, implying that Congo red is promising to serve as an effective and convenient probe for determining the self-assembly of GSH and copper ions. Furthermore, silica nanotubes are synthesized using the nanofibres as a template in a very simple way. The silica nanotubes can be lit up by biomolecule-templated metal nanoparticles or nanoclusters and emit bright fluorescence. This work will certainly open up new opportunities in fabricating a broad range of nanostructured materials with versatile functionalities.
- 23 August 2013
- Published by IOP Publishing in Nanotechnology
- Vol. 24 (37) , 375603
Lighting up silica nanotubes transcribed from the submicron structure of a metal–peptide hybrid
Fluorescent silica nanotubes are attracting increasing interest because of their versatile applicability in a range of diverse fields. By using sol-gel transcription of tetraethylorthosilicate (TEOS) from various soft templates, silica nanotubes can be conveniently prepared. Metal-peptide hybrids with well-defined nanostructures and outstanding functionalities are very interesting candidates to serve as templates. Herein, we demonstrate that glutathione (GSH) can act as a building block for a bioinspired structure with dimensions down to the nanoscale, based on specific interactions between metal ions and the peptide. Congo red is able to selectively stain the nanofibres obtained, and appears apple-green in colour, implying that Congo red is promising to serve as an effective and convenient probe for determining the self-assembly of GSH and copper ions. Furthermore, silica nanotubes are synthesized using the nanofibres as a template in a very simple way. The silica nanotubes can be lit up by biomolecule-templated metal nanoparticles or nanoclusters and emit bright fluorescence. This work will certainly open up new opportunities in fabricating a broad range of nanostructured materials with versatile functionalities.
- 8 August 2013
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 49 (79) , 9048-9050
Functional polypyrrole–silica composites as photothermal agents for targeted killing of bacteria
We demonstrate for the first time that PPy–SiO2–GTA composites can be used as efficient photothermal agents for killing pathogenic bacteria under NIR irradiation. The cell growth of both gram-positive and gram-negative bacteria targeted by PPy–SiO2–GTA composites could be inhibited effectively after photothermal treatment.
- 8 August 2013
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 49 (79) , 9048-9050
Functional polypyrrole–silica composites as photothermal agents for targeted killing of bacteria
We demonstrate for the first time that PPy–SiO2–GTA composites can be used as efficient photothermal agents for killing pathogenic bacteria under NIR irradiation. The cell growth of both gram-positive and gram-negative bacteria targeted by PPy–SiO2–GTA composites could be inhibited effectively after photothermal treatment.
Aptamer‐Directed Synthesis of Multifunctional Lanthanide‐Doped Porous Nanoprobes for Targeted Imaging and Drug Delivery
Multifunctional lanthanide‐doped porous nanoparticles are prepared via a facile one‐step solvothermal route by employing aptamers as the biotemplate. The nanoparticles feature excellent aqueous dispersibility and biospecific properties and could work as effective nanoprobes for targeted imaging and drug delivery. With aptamer being in principle available for any kind of target, this synthetic strategy may open the door to a new generation of nanoprobes for bioapplications such as time‐resolved biodetection, multimode bioimaging/biolabeling, and targeted cancer therapy.
Aptamer‐Directed Synthesis of Multifunctional Lanthanide‐Doped Porous Nanoprobes for Targeted Imaging and Drug Delivery
Multifunctional lanthanide‐doped porous nanoparticles are prepared via a facile one‐step solvothermal route by employing aptamers as the biotemplate. The nanoparticles feature excellent aqueous dispersibility and biospecific properties and could work as effective nanoprobes for targeted imaging and drug delivery. With aptamer being in principle available for any kind of target, this synthetic strategy may open the door to a new generation of nanoprobes for bioapplications such as time‐resolved biodetection, multimode bioimaging/biolabeling, and targeted cancer therapy.
- 25 June 2013
- Published by Wiley in Advanced Materials
- Vol. 25 (32) , 4452-4458
Hydrophobic Anticancer Drug Delivery by a 980 nm Laser‐Driven Photothermal Vehicle for Efficient Synergistic Therapy of Cancer Cells In Vivo
A novel 980 nm laser-driven hydrophobic anticancer drug-delivery platform based on hollow CuS nanoparticles is constructed in this work. The excellent synergistic therapy combining drug treatment and photothermal ablation of cancer cells both in vitro and in vivo is demonstrated, which opens up new opportunities for biological and medical applications.
- 25 June 2013
- Published by Wiley in Advanced Materials
- Vol. 25 (32) , 4452-4458
Hydrophobic Anticancer Drug Delivery by a 980 nm Laser‐Driven Photothermal Vehicle for Efficient Synergistic Therapy of Cancer Cells In Vivo
A novel 980 nm laser-driven hydrophobic anticancer drug-delivery platform based on hollow CuS nanoparticles is constructed in this work. The excellent synergistic therapy combining drug treatment and photothermal ablation of cancer cells both in vitro and in vivo is demonstrated, which opens up new opportunities for biological and medical applications.