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Gold Nanoframeworks with Mesopores for Raman-Photoacoustic Imaging and Photo-Chemo Tumor Therapy in the Second Near-Infrared Biowindow.

Advanced functional materials

Wang J, Sun J, Wang Y, Chou T, Zhang Q, Zhang B, Ren L, Wang H.
PMID: 34163312
Adv Funct Mater. 2020 Feb 26;30(9). doi: 10.1002/adfm.201908825. Epub 2020 Jan 08.

Gold-based nanostructures with tunable wavelength of localized surface plasmon resonance (LSPR) in the second near-infrared (NIR-II) biowindow receive increasing attention in phototheranostics. In view of limited progress on NIR-II gold nanostructures, a particular liposome template-guided route is explored to...

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Wang J, Sun J, Wang Y, et al. Gold Nanoframeworks with Mesopores for Raman-Photoacoustic Imaging and Photo-Chemo Tumor Therapy in the Second Near-Infrared Biowindow. Adv Funct Mater. 2020;30(9)doi: 10.1002/adfm.201908825.
Wang, J., Sun, J., Wang, Y., Chou, T., Zhang, Q., Zhang, B., Ren, L., & Wang, H. (2020). Gold Nanoframeworks with Mesopores for Raman-Photoacoustic Imaging and Photo-Chemo Tumor Therapy in the Second Near-Infrared Biowindow. Advanced functional materials, 30(9), . https://doi.org/10.1002/adfm.201908825
Wang, Jinping, et al. "Gold Nanoframeworks with Mesopores for Raman-Photoacoustic Imaging and Photo-Chemo Tumor Therapy in the Second Near-Infrared Biowindow." Advanced functional materials vol. 30,9 (2020). doi: https://doi.org/10.1002/adfm.201908825
Wang J, Sun J, Wang Y, Chou T, Zhang Q, Zhang B, Ren L, Wang H. Gold Nanoframeworks with Mesopores for Raman-Photoacoustic Imaging and Photo-Chemo Tumor Therapy in the Second Near-Infrared Biowindow. Adv Funct Mater. 2020 Feb 26;30(9). doi: 10.1002/adfm.201908825. Epub 2020 Jan 08. PMID: 34163312; PMCID: PMC8218930.
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NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy.

Bone

Schilling K, Brown E, Zhang X.
PMID: 34781049
Bone. 2022 Jan;154:116257. doi: 10.1016/j.bone.2021.116257. Epub 2021 Nov 13.

Two-photon fluorescence lifetime microscopy (2P-FLIM) is a non-invasive optical technique that can obtain cellular metabolism information based on the intrinsic autofluorescence lifetimes of free and enzyme-bound NAD(P)H, which reflect the metabolic state of single cells within the native microenvironment...

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Schilling K, Brown E, Zhang X. NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy. Bone. 2021;154:116257doi: 10.1016/j.bone.2021.116257.
Schilling, K., Brown, E., & Zhang, X. (2022). NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy. Bone, 154116257. https://doi.org/10.1016/j.bone.2021.116257
Schilling, Kevin, et al. "NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy." Bone vol. 154 (2022): 116257. doi: https://doi.org/10.1016/j.bone.2021.116257
Schilling K, Brown E, Zhang X. NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy. Bone. 2022 Jan;154:116257. doi: 10.1016/j.bone.2021.116257. Epub 2021 Nov 13. PMID: 34781049; PMCID: PMC8671374.
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Controlling Arteriogenesis and Mast Cells Are Central to Bioengineering Solutions for Critical Bone Defect Repair Using Allografts.

Bioengineering (Basel, Switzerland)

Antebi B, Zhang L, Sheyn D, Pelled G, Zhang X, Gazit Z, Schwarz EM, Gazit D.
PMID: 27141513
Bioengineering (Basel). 2016 Mar;3(1). doi: 10.3390/bioengineering3010006.

Although most fractures heal, critical defects in bone fail due to aberrant differentiation of mesenchymal stem cells towards fibrosis rather than osteogenesis. While conventional bioengineering solutions to this problem have focused on enhancing angiogenesis, which is required for bone...

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Antebi B, Zhang L, Sheyn D, et al. Controlling Arteriogenesis and Mast Cells Are Central to Bioengineering Solutions for Critical Bone Defect Repair Using Allografts. Bioengineering (Basel). 2016;3(1)doi: 10.3390/bioengineering3010006.
Antebi, B., Zhang, L., Sheyn, D., Pelled, G., Zhang, X., Gazit, Z., Schwarz, E. M., & Gazit, D. (2016). Controlling Arteriogenesis and Mast Cells Are Central to Bioengineering Solutions for Critical Bone Defect Repair Using Allografts. Bioengineering (Basel, Switzerland), 3(1), . https://doi.org/10.3390/bioengineering3010006
Antebi, Ben, et al. "Controlling Arteriogenesis and Mast Cells Are Central to Bioengineering Solutions for Critical Bone Defect Repair Using Allografts." Bioengineering (Basel, Switzerland) vol. 3,1 (2016). doi: https://doi.org/10.3390/bioengineering3010006
Antebi B, Zhang L, Sheyn D, Pelled G, Zhang X, Gazit Z, Schwarz EM, Gazit D. Controlling Arteriogenesis and Mast Cells Are Central to Bioengineering Solutions for Critical Bone Defect Repair Using Allografts. Bioengineering (Basel). 2016 Mar;3(1). doi: 10.3390/bioengineering3010006. PMID: 27141513; PMCID: PMC4851447.
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Nanomedicine-Enabled Modulation of Tumor Hypoxic Microenvironment for Enhanced Cancer Therapy.

Advanced therapeutics

Wang J, Zhang B, Sun J, Wang Y, Wang H.
PMID: 34277929
Adv Ther (Weinh). 2020 Jan;3(1). doi: 10.1002/adtp.201900083. Epub 2019 Sep 30.

Hypoxia is a common condition of solid tumors that is mainly caused by enhanced tumor proliferative activity and dysfunctional vasculature. In the treatment of hypoxic human solid tumors, many conventional therapeutic approaches (e.g., oxygen-dependent photodynamic therapy, anticancer drug-based chemotherapy...

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Wang J, Zhang B, Sun J, et al. Nanomedicine-Enabled Modulation of Tumor Hypoxic Microenvironment for Enhanced Cancer Therapy. Adv Ther (Weinh). 2019;3(1)doi: 10.1002/adtp.201900083.
Wang, J., Zhang, B., Sun, J., Wang, Y., & Wang, H. (2020). Nanomedicine-Enabled Modulation of Tumor Hypoxic Microenvironment for Enhanced Cancer Therapy. Advanced therapeutics, 3(1), . https://doi.org/10.1002/adtp.201900083
Wang, Jinping, et al. "Nanomedicine-Enabled Modulation of Tumor Hypoxic Microenvironment for Enhanced Cancer Therapy." Advanced therapeutics vol. 3,1 (2020). doi: https://doi.org/10.1002/adtp.201900083
Wang J, Zhang B, Sun J, Wang Y, Wang H. Nanomedicine-Enabled Modulation of Tumor Hypoxic Microenvironment for Enhanced Cancer Therapy. Adv Ther (Weinh). 2020 Jan;3(1). doi: 10.1002/adtp.201900083. Epub 2019 Sep 30. PMID: 34277929; PMCID: PMC8281934.
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NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy.

Bone

Schilling K, Brown E, Zhang X.
PMID: 34781049
Bone. 2022 Jan;154:116257. doi: 10.1016/j.bone.2021.116257. Epub 2021 Nov 13.

Two-photon fluorescence lifetime microscopy (2P-FLIM) is a non-invasive optical technique that can obtain cellular metabolism information based on the intrinsic autofluorescence lifetimes of free and enzyme-bound NAD(P)H, which reflect the metabolic state of single cells within the native microenvironment...

Cite
Schilling K, Brown E, Zhang X. NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy. Bone. 2021;154:116257doi: 10.1016/j.bone.2021.116257.
Schilling, K., Brown, E., & Zhang, X. (2022). NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy. Bone, 154116257. https://doi.org/10.1016/j.bone.2021.116257
Schilling, Kevin, et al. "NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy." Bone vol. 154 (2022): 116257. doi: https://doi.org/10.1016/j.bone.2021.116257
Schilling K, Brown E, Zhang X. NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy. Bone. 2022 Jan;154:116257. doi: 10.1016/j.bone.2021.116257. Epub 2021 Nov 13. PMID: 34781049.
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NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy.

Bone

Schilling K, Brown E, Zhang X.
PMID: 34781049
Bone. 2022 Jan;154:116257. doi: 10.1016/j.bone.2021.116257. Epub 2021 Nov 13.

Two-photon fluorescence lifetime microscopy (2P-FLIM) is a non-invasive optical technique that can obtain cellular metabolism information based on the intrinsic autofluorescence lifetimes of free and enzyme-bound NAD(P)H, which reflect the metabolic state of single cells within the native microenvironment...

Cite
Schilling K, Brown E, Zhang X. NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy. Bone. 2021;154:116257doi: 10.1016/j.bone.2021.116257.
Schilling, K., Brown, E., & Zhang, X. (2022). NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy. Bone, 154116257. https://doi.org/10.1016/j.bone.2021.116257
Schilling, Kevin, et al. "NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy." Bone vol. 154 (2022): 116257. doi: https://doi.org/10.1016/j.bone.2021.116257
Schilling K, Brown E, Zhang X. NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy. Bone. 2022 Jan;154:116257. doi: 10.1016/j.bone.2021.116257. Epub 2021 Nov 13. PMID: 34781049.
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NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy.

Bone

Schilling K, Brown E, Zhang X.
PMID: 34781049
Bone. 2022 Jan;154:116257. doi: 10.1016/j.bone.2021.116257. Epub 2021 Nov 13.

Two-photon fluorescence lifetime microscopy (2P-FLIM) is a non-invasive optical technique that can obtain cellular metabolism information based on the intrinsic autofluorescence lifetimes of free and enzyme-bound NAD(P)H, which reflect the metabolic state of single cells within the native microenvironment...

Cite
Schilling K, Brown E, Zhang X. NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy. Bone. 2021;154:116257doi: 10.1016/j.bone.2021.116257.
Schilling, K., Brown, E., & Zhang, X. (2022). NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy. Bone, 154116257. https://doi.org/10.1016/j.bone.2021.116257
Schilling, Kevin, et al. "NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy." Bone vol. 154 (2022): 116257. doi: https://doi.org/10.1016/j.bone.2021.116257
Schilling K, Brown E, Zhang X. NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy. Bone. 2022 Jan;154:116257. doi: 10.1016/j.bone.2021.116257. Epub 2021 Nov 13. PMID: 34781049; PMCID: PMC8671374.
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Construction of vascular graft with circumferentially oriented microchannels for improving artery regeneration.

Biomaterials

Wu P, Wang L, Li W, Zhang Y, Wu Y, Zhi D, Wang H, Wang L, Kong D, Zhu M.
PMID: 32155476
Biomaterials. 2020 Mar 04;242:119922. doi: 10.1016/j.biomaterials.2020.119922. Epub 2020 Mar 04.

Design and fabrication of scaffolds with three-dimensional (3D) topological cues inducing regeneration of the neo-tissue comparable to native one remains a major challenge in both scientific and clinical fields. Here, we developed a well-designed vascular graft with 3D highly...

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Wu P, Wang L, Li W, et al. Construction of vascular graft with circumferentially oriented microchannels for improving artery regeneration. Biomaterials. 2020;242:119922doi: 10.1016/j.biomaterials.2020.119922.
Wu, P., Wang, L., Li, W., Zhang, Y., Wu, Y., Zhi, D., Wang, H., Wang, L., Kong, D., & Zhu, M. (2020). Construction of vascular graft with circumferentially oriented microchannels for improving artery regeneration. Biomaterials, 242119922. https://doi.org/10.1016/j.biomaterials.2020.119922
Wu, Pingli, et al. "Construction of vascular graft with circumferentially oriented microchannels for improving artery regeneration." Biomaterials vol. 242 (2020): 119922. doi: https://doi.org/10.1016/j.biomaterials.2020.119922
Wu P, Wang L, Li W, Zhang Y, Wu Y, Zhi D, Wang H, Wang L, Kong D, Zhu M. Construction of vascular graft with circumferentially oriented microchannels for improving artery regeneration. Biomaterials. 2020 Mar 04;242:119922. doi: 10.1016/j.biomaterials.2020.119922. Epub 2020 Mar 04. PMID: 32155476; PMCID: PMC7483276.
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NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy.

Bone

Schilling K, Brown E, Zhang X.
PMID: 34781049
Bone. 2022 Jan;154:116257. doi: 10.1016/j.bone.2021.116257. Epub 2021 Nov 13.

Two-photon fluorescence lifetime microscopy (2P-FLIM) is a non-invasive optical technique that can obtain cellular metabolism information based on the intrinsic autofluorescence lifetimes of free and enzyme-bound NAD(P)H, which reflect the metabolic state of single cells within the native microenvironment...

Cite
Schilling K, Brown E, Zhang X. NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy. Bone. 2021;154:116257doi: 10.1016/j.bone.2021.116257.
Schilling, K., Brown, E., & Zhang, X. (2022). NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy. Bone, 154116257. https://doi.org/10.1016/j.bone.2021.116257
Schilling, Kevin, et al. "NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy." Bone vol. 154 (2022): 116257. doi: https://doi.org/10.1016/j.bone.2021.116257
Schilling K, Brown E, Zhang X. NAD(P)H autofluorescence lifetime imaging enables single cell analyses of cellular metabolism of osteoblasts in vitro and in vivo via two-photon microscopy. Bone. 2022 Jan;154:116257. doi: 10.1016/j.bone.2021.116257. Epub 2021 Nov 13. PMID: 34781049.
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Recent advances in porous nanostructures for cancer theranostics.

Nano today

Wang J, Zhang B, Sun J, Hu W, Wang H.
PMID: 33897805
Nano Today. 2021 Jun;38. doi: 10.1016/j.nantod.2021.101146. Epub 2021 Apr 08.

Porous nanomaterials with high surface area, tunable porosity, and large mesopores have recently received particular attention in cancer therapy and imaging. Introduction of additional pores to nanostructures not only endows the tunability of optoelectronic and optical features optimal for...

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Wang J, Zhang B, Sun J, et al. Recent advances in porous nanostructures for cancer theranostics. Nano Today. 2021;38doi: 10.1016/j.nantod.2021.101146.
Wang, J., Zhang, B., Sun, J., Hu, W., & Wang, H. (2021). Recent advances in porous nanostructures for cancer theranostics. Nano today, 38. https://doi.org/10.1016/j.nantod.2021.101146
Wang, Jinping, et al. "Recent advances in porous nanostructures for cancer theranostics." Nano today vol. 38 (2021). doi: https://doi.org/10.1016/j.nantod.2021.101146
Wang J, Zhang B, Sun J, Hu W, Wang H. Recent advances in porous nanostructures for cancer theranostics. Nano Today. 2021 Jun;38. doi: 10.1016/j.nantod.2021.101146. Epub 2021 Apr 08. PMID: 33897805; PMCID: PMC8059603.
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Showing 1 to 10 of 10 entries