TY - JOUR
T1 - In situ sprayed NIR-responsive, analgesic black phosphorus-based gel for diabetic ulcer treatment
AU - Ouyang, Jiang
AU - Ji, Xiaoyuan
AU - Zhang, Xingcai
AU - Feng, Chan
AU - Tang, Zhongmin
AU - Kong, Na
AU - Xie, Angel
AU - Wang, Junqing
AU - Sui, Xinbing
AU - Deng, Liu
AU - Liu, Younian
AU - Kim, Jong Seung
AU - Cao, Yihai
AU - Tao, Wei
N1 - Funding Information:
ACKNOWLEDGMENTS. This work is supported by Harvard Medical School/ Brigham and Women’s Hospital Department of Anesthesiology-Basic Scientist Grant 2420 BPA075 (to W.T.), Stepping Strong Center Award for Trauma Innovation Grant 113548, and Center for Nanomedicine Research Fund 2019A014810 (to W.T.). W.T. is a recipient of Khoury Innovation Award 2020A003219 and American Heart Association Collaborative Sciences Award 2018A004190. W.T. also received a start-up package (for three years) from the Department of Anesthesiology, Perioperative and Pain Medicine to establish his independent research laboratory at Harvard Medical School and Brigham and Women’s Hospital. We thank our department for this generous support.
Publisher Copyright:
© 2020 National Academy of Sciences. All rights reserved.
PY - 2020/11/17
Y1 - 2020/11/17
N2 - The treatment of diabetic ulcer (DU) remains a major clinical challenge due to the complex wound-healing milieu that features chronic wounds, impaired angiogenesis, persistent pain, bacterial infection, and exacerbated inflammation. A strategy that effectively targets all these issues has proven elusive. Herein, we use a smart black phosphorus (BP)-based gel with the characteristics of rapid formation and near-infrared light (NIR) responsiveness to address these problems. The in situ sprayed BP-based gel could act as 1) a temporary, biomimetic “skin” to temporarily shield the tissue from the external environment and accelerate chronic wound healing by promoting the proliferation of endothelial cells, vascularization, and angiogenesis and 2) a drug “reservoir” to store therapeutic BP and pain-relieving lidocaine hydrochloride (Lid). Within several minutes of NIR laser irradiation, the BP-based gel generates local heat to accelerate microcirculatory blood flow, mediate the release of loaded Lid for “on-demand” pain relief, eliminate bacteria, and reduce inflammation. Therefore, our study not only introduces a concept of in situ sprayed, NIR-responsive pain relief gel targeting the challenging wound-healing milieu in diabetes but also provides a proof-of-concept application of BP-based materials in DU treatment.
AB - The treatment of diabetic ulcer (DU) remains a major clinical challenge due to the complex wound-healing milieu that features chronic wounds, impaired angiogenesis, persistent pain, bacterial infection, and exacerbated inflammation. A strategy that effectively targets all these issues has proven elusive. Herein, we use a smart black phosphorus (BP)-based gel with the characteristics of rapid formation and near-infrared light (NIR) responsiveness to address these problems. The in situ sprayed BP-based gel could act as 1) a temporary, biomimetic “skin” to temporarily shield the tissue from the external environment and accelerate chronic wound healing by promoting the proliferation of endothelial cells, vascularization, and angiogenesis and 2) a drug “reservoir” to store therapeutic BP and pain-relieving lidocaine hydrochloride (Lid). Within several minutes of NIR laser irradiation, the BP-based gel generates local heat to accelerate microcirculatory blood flow, mediate the release of loaded Lid for “on-demand” pain relief, eliminate bacteria, and reduce inflammation. Therefore, our study not only introduces a concept of in situ sprayed, NIR-responsive pain relief gel targeting the challenging wound-healing milieu in diabetes but also provides a proof-of-concept application of BP-based materials in DU treatment.
KW - Analgesic
KW - Black phosphorus
KW - Diabetic ulcer
KW - Fibrin gel
KW - Wound healing
UR - http://www.scopus.com/inward/record.url?scp=85096159645&partnerID=8YFLogxK
U2 - 10.1073/pnas.2016268117
DO - 10.1073/pnas.2016268117
M3 - Article
C2 - 33139557
AN - SCOPUS:85096159645
SN - 0027-8424
VL - 117
SP - 28667
EP - 28677
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 46
ER -