Lian-Di Kan

Dr. Lian-Di Kan

Department of Pharmacy, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University
orcid

Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

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

Representative Publications

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1 February 2017 in Journal of Ethnopharmacology
Verified
Journal Article
Closed access
LLLiu-Cheng Li
Liu-Cheng Li
LKLian-Di Kan
Lian-Di Kan

8 August 2017 in Frontiers in Pharmacology
Verified
Journal Article
Open access
LLLiu-Cheng Li
Liu-Cheng Li
LXLiang Xu
Liang Xu
YHYan Hu
Yan Hu
WCWen-Jie Cui
Wen-Jie Cui
WCWen-Hui Cui
Wen-Hui Cui
LKLian-Di Kan
Lian-Di Kan
Pulmonary fibrosis is a devastating lung disorder with mysterious pathogenesis and limited treatment options. It is well recognized that the uncontrolled proliferation of lung fibroblasts and differentiation of fibroblasts into myofibroblasts excessively produce extracellular matrix (ECM) proteins which contribute to the fibrosis change of the lungs. Thus, blocking ECM accumulation would delay fibrosis progression. In this study, we observed the effects of astragaloside IV (ASV) (10 mg/kg/d) on ECM proteins in bleomycin (BLM, 5 mg/kg)-treated rats. Our results showed that ASV not only ameliorated BLM-induced body weight loss, lung coefficient increase, histological changes and collagen secretion, but also reduced the levels of type III collagen (Col-III) in lung homogenate, laminin (LN) and hyaluronic acid (HA) in serum, as well as hydroxyproline (HYP) in lung tissue. Besides, ASV significantly down-regulated the levels of high-mobility group box1 (HMGB1) in serum and lung tissue, and inhibited the up-regulated expression of α-SMA (marker of myofibroblasts) in the lungs. Taken together, these findings indicate that ASV attenuates BLM-induced ECM deposition, supporting its use as a promising candidate to treat lung fibrosis.

1 October 2020 in Biomedicine & Pharmacotherapy
Verified
Journal Article
Open access
LLLiu-Cheng Li
Liu-Cheng Li
ZZZhi-Hui Zhang
Zhi-Hui Zhang
WZWen-Cheng Zhou
Wen-Cheng Zhou
JCJie Chen
Jie Chen
HJHua-Qian Jin
Hua-Qian Jin
LKLian-Di Kan
Lian-Di Kan
An outbreak of Coronavirus Disease 2019 (COVID-19) which was infected by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), is still spreading and has led to unprecedented health emergency over the world. Though no specific drug has been developed so far, emerging agents have been confirmed effective or potentially beneficial to restrain it. Lianhua Qingwen (LHQW) is a commonly used Chinese medical preparation to treat viral influenza, including in the fight against SARS in 2002-2003 in China. Recent data also showed that LHQW played a vigorous role in COVID-19 treatment. This review will elucidate the pre-clinical and clinical evidence of LHQW in lung protection and antiviral activities, and provide timely data delivery for the exploration of effective treatment strategies in the therapy of COVID-19. The research data were obtained from the academic databases (up to August 8, 2020) including Pubmed, CNKI and Web of Science, on ethnobotany and ethno medicines. The search keywords for screening the literature information were "virus", "COVID-19", or "SARS-CoV-2", and "Lianhua Qingwen". The documents were filtered and summarized for final evaluation. The collected evidence demonstrated that LHQW exhibited benefits against COVID-19. Impressively, LHQW in conjunction with conventional treatment could significantly improve COVID-19 patients as a synergetic strategy. The mechanisms were mainly involved the antiviral activity, and regulation of inflammation response as well as immune function. Although the data were far from adequate, the latest advances had shown the benefits of LHQW in COVID-19, especially in combination with other antiviral drugs. This review provides comprehensive evidence of LHQW as a complementary strategy for treating COVID-19. Nevertheless, imperious researches should be conducted to clarify the unconfirmed effects, regulatory mechanisms and adverse reactions of LHQW in treating COVID-19 by means of well designed randomized controlled trials.

1 January 2019 in Revista Española de Enfermedades Digestivas
Verified
Journal Article
Closed access
JYJie Ying
Jie Ying
LLLiu-Cheng Li
Liu-Cheng Li
CWCui-Yun Wu
Cui-Yun Wu
ZYZhen-Wei Yu
Zhen-Wei Yu
LKLian-Di Kan
Lian-Di Kan
Proton pump inhibitors (PPI) have been widely used in the clinic but inappropriate prescribing has also increased dramatically. to describe the prescribing patterns and assess the appropriateness of the prescribed PPI use in 45 hospitals in China. PPI prescriptions for non-hospitalized patients were collected from hospitals in Beijing, Chengdu, Guangzhou and Hangzhou of China over a 40-day period in 2016. These data were analyzed using the prescription number, proportion and economic indicators (defined daily dose system [DDD], defined daily cost [DDC] and drug utilization index [DUI]). The evaluation criteria of PPI use was based on Martindale: The Complete Drug Reference, New Materia Medica and drug instructions. in total, 357,687 prescriptions using oral PPI and 38,216 prescriptions using injectable PPI were assessed. The average age of PPI users was 53 years. The most commonly used oral PPI was rabeprazole, while the most common injectable PPI was pantoprazole. The DDD of oral rabeprazole and DDC of injectable rabeprazole were the highest. Meanwhile, only the DUI values of oral rabeprazole, lansoprazole and ilaprazole were less than 1.0. The clinical diagnosis of some users included well identified risky comorbidities such as kidney disease (2.9%). Furthermore, between 32.6% and 56.8% of the PPI prescriptions were used for inappropriate indications. this survey demonstrated that PPI use was accompanied by unapproved indications and excessive dosages. Comprehensive measures are urgently needed to improve PPI use and reduce unnecessary drug costs.

26 December 2022 in Drug Development Research
Verified
Journal Article
Closed access
YWYu‐Zhen Wang
Yu‐Zhen Wang
JCJie Chen
Jie Chen
SPShi‐Qin Pei
Shi‐Qin Pei
CWChen Wang
Chen Wang
GHGang Han
Gang Han
LLLiu-Cheng Li
Liu-Cheng Li

1 January 2021 in Drug Design, Development and Therapy
Verified
Journal Article
Open access
PDF file
LLLiu-Cheng Li
Liu-Cheng Li
YHYong-Yue Han
Yong-Yue Han
ZZZhi-Hui Zhang
Zhi-Hui Zhang
WZWen-Cheng Zhou
Wen-Cheng Zhou
HFHong-Mei Fang
Hong-Mei Fang
LKLian-Di Kan
Lian-Di Kan
Chronic obstructive pulmonary disease (COPD) is the fourth leading cause of death across the globe. Its repeated exacerbation will seriously worsen the quality of life, aggravate the patients’ symptoms, and bring a heavy burden on the patients and the society. Understanding the current status of drug therapy and the role of pharmaceutical care is essential for the management of COPD. In addition to the drugs already on the market, recent clinical trials also show that emerging novel drugs for treating COPD are being developed to prevent the symptoms, reduce the frequency of acute exacerbation, and improve the quality of life. Recent progress in new drug research should lead to novel treatment options for COPD patients in future clinical practice. The pharmaceutical care has shown significantly favourable impacts on addressing drug-related problems, supporting its vital role in the management of COPD, especially when there are a wide range of therapeutic agents. This review not only provides an overview of current treatment strategies but also further underlines the importance of new drug development and pharmaceutical care for patients with COPD.