Qifa Ye

Qifa Ye


Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2016 in Carbohydrate Polymers
Verified
Journal Article
Closed access
NPNa Peng
Na Peng
YWYanfeng Wang
Yanfeng Wang
QYQifa Ye
Qifa Ye
LLLei Liang
Lei Liang
YAYuxing An
Yuxing An
Chunyu  ChangChunyu Chang
Chunyu Chang

1 October 2017 in Carbohydrate Polymers
Verified
Journal Article
Closed access
SWShuangquan Wu
Shuangquan Wu
BDBo Duan
Bo Duan
ALAng Lu
Ang Lu
YWYanfeng Wang
Yanfeng Wang
QYQifa Ye
Qifa Ye
LZLina Zhang
Lina Zhang

21 January 2023 in Carbohydrate Polymers
Verified
Journal Article
Closed access
HCHankun Cao
Hankun Cao
DXDu Xiang
Du Xiang
XZXin Zhou
Xin Zhou
PYPengpeng Yue
Pengpeng Yue
YZYongkang Zou
Yongkang Zou
QYQifa Ye
Qifa Ye

4 May 2020 in American Journal of Transplantation
Verified
Journal Article
Open access
ZZZibiao Zhong
Zibiao Zhong
QZQiuyan Zhang
Qiuyan Zhang
HXHaoyang Xia
Haoyang Xia
AWAiping Wang
Aiping Wang
WLWenjin Liang
Wenjin Liang
QYQifa Ye
Qifa Ye
Over 1 000 000 cases of coronavirus disease 2019 (COVID-19) have been confirmed since the worldwide outbreak began. Not enough data on infected solid organ transplant (SOT) recipients are available, especially data about the management of immunosuppressants. We report two cases of COVID-19 in two transplant recipients, with different treatments and prognoses. The first patient received liver transplantation due to hepatitis B virus-related hepatocellular carcinoma and was confirmed to have COVID-19 9 days later. Following a treatment regimen consisting of discontinued immunosuppressant use and low-dose methylprednisolone-based therapy, the patient developed acute rejection but eventually recovered. The other patient had undergone a renal transplant from a living-related donor 17 years ago, and was admitted to the hospital because of persistent fever. This patient was also diagnosed with COVID-19. His treatment regimen consisted of reduced immunosuppressant use. No signs of rejection were observed during the regimen. In the end, the patient successfully recovered from COVID-19. These effectively treated cases can provide a basis for immunosuppressant management of COVID-19-positive SOT recipients.

4 May 2024 in Carbohydrate Polymers
Verified
Journal Article
Closed access
LMLanxin Mu
Lanxin Mu
LWLiqin Wu
Liqin Wu
SWShuangquan Wu
Shuangquan Wu
QYQifa Ye
Qifa Ye
ZZZibiao Zhong
Zibiao Zhong

22 March 2017 in Journal of Materials Chemistry B
Verified
Journal Article
Closed access
PDF file
SWShuangquan Wu
Shuangquan Wu
BDBo Duan
Bo Duan
XZXianpeng Zeng
Xianpeng Zeng
ALAng Lu
Ang Lu
XXXiaojuan Xu
Xiaojuan Xu
LZLina Zhang
Lina Zhang
Excess bilirubin often evokes hepatobiliary system dysfunction. In the present work, we developed an efficient, safe and blood compatible adsorbent for bilirubin removal from human blood. In view of the highly effective adsorption of carbon nanotubes (CNTs) on bilirubin but with many side effects, and good biocompatibility of chitin but with low efficiency for bilirubin removal, new chitin/carbon nanotube (Ch/CNT) nanofibrous microspheres were constructed from chitin solution in NaOH/urea aqueous system by blending with CNTs. The results of AFM, SEM, and TEM demonstrated that the CNTs were dispersed well in the chitin matrix, and the chitin nanofibers intertwined with CNTs to form hybrid chitin/CNT nanofibers and then weaved into a 3D interconnected network architecture. Moreover, lysine (Lys), a highly specific ligand for bilirubin, was immobilized tightly to the hybrid microspheres to obtain Ch/CNT/Lys. The resultant microspheres possessed large surface area and hierarchical pores including mesopores and micropores, which could allow bilirubin to enter easily and store, leading to highly efficient adsorption. The Ch/CNT/Lys microspheres exhibited excellent bilirubin adsorption property (107.2 mg g−1) and efficient bilirubin clearance rate from real hyperbilirubinemia plasma competing with protein, as well as good cell affinity and blood compatibility, as a result of the combination of the high adsorption of CNTs and inherent biocompatibility of chitin and lysine. Therefore, an effective strategy to develop a novel biocompatible and blood compatible bilirubin adsorbent is provided, showing potential applications for hemoperfusion in blood purified therapy.