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Research on classification diagnosis model of psoriasis based on deep residual network 基于深度残差网络的银屑病分类诊断模型研究
Q3 Medicine Pub Date : 2021-06-01 DOI: 10.1016/j.dcmed.2021.06.003
Li Peng , Yi Na , Ding Changsong , L.I. Sheng , Min Hui

Objective

A classification and diagnosis model for psoriasis based on deep residual network is proposed in this paper. Which using deep learning technology to classify and diagnose psoriasis can help reduce the burden of doctors, simplify the diagnosis and treatment process, and improve the quality of diagnosis.

Methods

Firstly, data enhancement, image resizings, and TFRecord coding are used to preprocess the input of the model, and then a 34-layer deep residual network (ResNet-34) is constructed to extract the characteristics of psoriasis. Finally, we used the Adam algorithm as the optimizer to train ResNet-34, used cross-entropy as the loss function of ResNet-34 in this study to measure the accuracy of the model, and obtained an optimized ResNet-34 model for psoriasis diagnosis.

Results

The experimental results based on k-fold cross validation show that the proposed model is superior to other diagnostic methods in terms of recall rate, F1-score and ROC curve.

Conclusion

The ResNet-34 model can achieve accurate diagnosis of psoriasis, and provide technical support for data analysis and intelligent diagnosis and treatment of psoriasis.

目的建立一种基于深度残差网络的银屑病分类诊断模型。其中利用深度学习技术对牛皮癣进行分类诊断,有助于减轻医生负担,简化诊疗流程,提高诊断质量。方法首先采用数据增强、图像调整大小、TFRecord编码等方法对模型输入进行预处理,然后构建34层深度残差网络(ResNet-34)提取银屑病特征。最后,我们使用Adam算法作为优化器对ResNet-34进行训练,并在本研究中使用交叉熵作为ResNet-34的损失函数来衡量模型的准确性,得到了优化后的ResNet-34银屑病诊断模型。结果基于k-fold交叉验证的实验结果表明,该模型在召回率、f1评分和ROC曲线上均优于其他诊断方法。结论ResNet-34模型可实现银屑病的准确诊断,为银屑病的数据分析和智能化诊疗提供技术支持。
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引用次数: 9
Novel pyrimidine-benzimidazole hybrids with antibacterial and antifungal properties and potential inhibition of SARS-CoV-2 main protease and spike glycoprotein 新型嘧啶-苯并咪唑复合物具有抗菌和抗真菌特性,并可能抑制SARS-CoV-2主要蛋白酶和刺突糖蛋白
Q3 Medicine Pub Date : 2021-06-01 DOI: 10.1016/j.dcmed.2021.06.004
Sharuk Khan , Mayura Kale , Falak Siddiqui , Nitin Nema

Objective

The study aimed to synthesize and characterize pyrimidine-linked benzimidazole hybrids, define their antimicrobial and antifungal activities in vitro, and determine their ability to inhibit the main protease and spike glycoprotein of SARS-CoV-2.

Methods

The ability of the synthesized compounds to inhibit the main protease and spike glycoprotein inhibitory of SARS-CoV-2 was investigated by assessing their mode of binding to the allosteric site of the enzyme using molecular docking. The structures of pyrimidine-linked benzimidazole derivatives synthesized with microwave assistance were confirmed by spectral analysis. Antibacterial and antifungal activities were determined by broth dilution.

Results

Gram-negative bateria (Escherichia coli and Pseudomonas aeruginosa) were more sensitive than gram-positive bateria (Staphylococcus aureus and Streptococcus pyogenes) to the derivatives. Candida albicans was sensitive to the derivatives at a minimal inhibitory concentration (MIC) of 250 μg/mL. The novel derivatives had better binding affinity (kcal/mol) than nelfinavir, lopinavir, ivermectin, remdesivir, and favipiravir, which are under investigation as treatment for SARS-CoV-2 infection. Compounds 2c, 2e, and 2g formed four hydrogen bonds with the active cavity of the main protease. Many derivatives had good binding affinity for the RBD of the of SARS-CoV-2 spike glycoprotein with the formation of up to four hydrogen bonds.

Conclusion

We synthesized novel pyrimidine-linked benzi-midazole derivatives that were potent antimicrobial agents with ability to inhibit the SARS-CoV-2 spike glycoprotein. Understanding the pharmacophore features of the main protease and spike glycoprotein offers much scope for the development of more potent agents. We plan to optimize the properties of the derivatives using models in vivo and in vitro so that they will serve as more effective therapeutic options against bacterial and SARS-CoV-2 infections.

目的合成并表征嘧啶联苯并咪唑杂合物,确定其体外抗菌和抗真菌活性,并测定其对SARS-CoV-2主要蛋白酶和刺突糖蛋白的抑制能力。方法采用分子对接的方法,评价合成的化合物与SARS-CoV-2酶的变构位点的结合方式,研究其对主要蛋白酶和刺突糖蛋白抑制的抑制能力。微波辅助合成的嘧啶连接苯并咪唑衍生物的结构经波谱分析证实。用肉汤稀释法测定其抑菌和抗真菌活性。结果革兰氏阴性菌(大肠杆菌和铜绿假单胞菌)对该衍生物的敏感性高于革兰氏阳性菌(金黄色葡萄球菌和化脓性链球菌)。白色念珠菌在最低抑菌浓度(MIC)为250 μg/mL时对其敏感。与正在研究的奈非那韦、洛匹那韦、伊维菌素、瑞德西韦和法匹拉韦相比,新型衍生物具有更好的结合亲和力(kcal/mol)。化合物2c、2e和2g与主蛋白酶的活性空腔形成4个氢键。许多衍生物与SARS-CoV-2刺突糖蛋白的RBD具有良好的结合亲和力,形成多达4个氢键。结论我们合成了一种新的嘧啶连接的苯并咪唑衍生物,具有抑制SARS-CoV-2刺突糖蛋白的活性。了解主要蛋白酶和刺突糖蛋白的药效团特征为开发更有效的药物提供了很大的空间。我们计划利用体内和体外模型优化衍生物的特性,使其成为对抗细菌和SARS-CoV-2感染的更有效的治疗选择。
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引用次数: 24
Quality 4.0 technologies to enhance traditional Chinese medicine for overcoming healthcare challenges during COVID-19 “品质4.0”技术提升中医药,应对新冠疫情期间的医疗挑战
Q3 Medicine Pub Date : 2021-06-01 DOI: 10.1016/j.dcmed.2021.06.001
Abid Haleem , Mohd Javaid , Ravi Pratap Singh , Rajiv Suman

The Quality 4.0 concept is derived from the industrial fourth revolution, i.e., Industry 4.0. Quality 4.0 is the future of quality, where new digital and disruptive technologies are used to maintain quality in organizations. It is also suitable for traditional Chinese medicine (TCM) to maintain quality. This quality revolution aims to improve industrial and service sectors’ quality by incorporating emerging technologies to connect physical systems with the natural world. The proposed digital philosophy can update and enhance the entire TCM treatment methodology to become more effective and attractive in the current competitive structure of the pharmaceutical and clinical industries. Thus, in healthcare, this revolution empowers quality treatment during the COVID-19 pandemic. There is a major requirement in healthcare to maintain the quality of medical tools, equipment, and treatment processes during a pandemic. Digital technologies can widely be used to provide innovative products and services with excellent quality for TCM. In this paper, we discuss the significant role of Quality 4.0 and how it can be used to maintain healthcare quality and fulfill challenges during the pandemic. Additionally, we discuss 10 significant applications of Quality 4.0 in healthcare during the COVID-19 pandemic. These technologies will provide unique benefits to maintain the quality of TCM throughout the treatment process. With Quality 4.0, quality can be maintained using innovative and advanced digital technologies.

质量4.0概念源于第四次工业革命,即工业4.0。质量4.0是质量的未来,新的数字和颠覆性技术被用来保持组织的质量。它也适用于中药(TCM)保持质量。这次质量革命旨在通过将物理系统与自然世界连接起来的新兴技术,提高工业和服务部门的质量。所提出的数字哲学可以更新和增强整个中医治疗方法,使其在当前制药和临床行业的竞争结构中变得更加有效和有吸引力。因此,在医疗保健领域,这一革命为COVID-19大流行期间的高质量治疗提供了支持。在大流行期间保持医疗工具、设备和治疗过程的质量是医疗保健的主要要求。数字技术可以广泛应用,为中医药提供创新、优质的产品和服务。在本文中,我们讨论了质量4.0的重要作用,以及如何使用它来保持医疗质量并应对大流行期间的挑战。此外,我们还讨论了在COVID-19大流行期间质量4.0在医疗保健领域的10个重要应用。这些技术将为在整个治疗过程中保持中药质量提供独特的好处。在Quality 4.0中,可以使用创新和先进的数字技术来保持质量。
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引用次数: 4
Protective effect of notoginsenoside and tanshinone IIA on inflammation-related colorectal cancer mice and the inhibition effect on COX-2 expression 三七皂苷和丹参酮IIA对炎症相关性结直肠癌小鼠的保护作用及对COX-2表达的抑制作用
Q3 Medicine Pub Date : 2021-03-01 DOI: 10.1016/j.dcmed.2021.03.007
Cao Wen , Zhou Xiaoqing

Objective

To explore the preventive effects and possible me-chanisms of action of notoginsenoside (NGS) and tanshinone IIA (TSN) in inflammation-related colorectal cancer (IRCC) in mice.

Methods

Eighty-eight male C57BL/6 mice were randomly assigned to 11 groups (n = 8 each group). Azomethane oxide + dextran sulfate (AOM + DSS) model control (model), NGS low-dose (l-NGS), NGS medium-dose (m-NGS), NGS high-dose (h-NGS), TSN low-dose (l-TSN), TSN medium-dose (m-TSN), TSN high-dose (h-TSN), (NGS + TSN) low-dose [l-(NGS + TSN)], (NGS + TSN) medium-dose [m-(NGS + TSN)], (NGS+TSN) high-dose [h-(NGS + TSN)], and blank groups were established. The first 10 groups were intraperitoneally injected with AOM to induce inflammatory colon cancer, whereas the blank group was intraperitoneally injected with 0.9% NaCl solution. The first 10 groups drank a 2.5% sodium DSS aqueous solution continuously from day 5 for three cycles (one cycle: five days, every three weeks), and the blank group was allowed free access to water. Drug groups were administered NGS (low, medium, or high dose), TSN (low, medium, or high dose), or NGS + TSN (low, medium, or high dose), and the model and blank groups were administered saline by lavage until the end of the experiment. The general activity, body weight, and survival rate of and incidence of adenocarcinoma in mice were detected and the expression of cyclooxygenase 2 (COX-2) was detected by immunohistochemistry.

Results

(1) The survival rate of mice with IRCC in the h-NGS, m-TSN, h-TSN, m-(NGS + TSN), and h-(NGS + TSN) groups was significantly increased than that in other groups (P < 0.05). (2) The incidence of tumors in the h-(NGS + TSN), m-TSN, and l-NGS groups was significantly lower than that in the model group (P < 0.05). (3) The expression level of COX-2 in tumor tissues of mice in the m-(NGS + TSN) and h-(NGS + TSN) groups was significantly lower than that in the model group (P < 0.05).

Conclusion

Tumor formation was inhibited by m-TSN and h-(NGS + TSN) treatments in mice with IRCC, and h-(NGS + TSN) treatment inhibited the COX-2 pathway.

目的探讨三七皂苷(NGS)和丹参酮IIA (TSN)对小鼠炎症相关性结直肠癌(IRCC)的预防作用及其可能的作用机制。方法雄性C57BL/6小鼠88只,随机分为11组,每组8只。建立偶氮甲烷氧化物+葡聚糖硫酸盐(AOM + DSS)模型对照(model)、NGS低剂量(l-NGS)、NGS中剂量(m-NGS)、NGS高剂量(h-NGS)、TSN低剂量(l-TSN)、TSN中剂量(m-TSN)、(NGS+TSN)中剂量[m-(NGS +TSN)]、(NGS+TSN)高剂量[h-(NGS +TSN)]和空白组。前10组腹腔注射AOM诱导炎性结肠癌,空白组腹腔注射0.9% NaCl溶液。前10组从第5天开始连续饮用2.5% DSS钠水溶液,共3个周期(1个周期:5天,每3周),空白组自由饮水。给药组分别给予NGS(低、中、高剂量)、TSN(低、中、高剂量)或NGS + TSN(低、中、高剂量),模型组和空白组灌胃生理盐水至实验结束。结果(1)h-NGS、m-TSN、h-TSN、m-(NGS + TSN)、h-(NGS + TSN)、h-(NGS + TSN)组IRCC小鼠的存活率显著高于其他各组(P <0.05)。(2) h-(NGS + TSN)、m-TSN、l-NGS组肿瘤发生率均显著低于模型组(P <0.05)。(3) m-(NGS + TSN)和h-(NGS + TSN)组小鼠肿瘤组织中COX-2的表达水平均显著低于模型组(P <0.05)。结论m-TSN和h-(NGS + TSN)处理可抑制IRCC小鼠的肿瘤形成,h-(NGS + TSN)处理可抑制COX-2通路。
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引用次数: 3
Linarin ameliorates innate inflammatory response in an experimental dry eye model via modulation of the NLRP3 inflammasome Linarin通过调节NLRP3炎性体改善实验性干眼模型中的先天炎症反应
Q3 Medicine Pub Date : 2021-03-01 DOI: 10.1016/j.dcmed.2021.03.006
Chen Mei , Li Jie , Peng Jun , Huang Yu , Ouyang Weijie , Liu Xiaoqing , Shen Zhibin , Li Changdong , Wang Yi , Peng Qinghua

Objective

To investigate the effect and mechanism of linarin (LA) in an experimental dry eye model

Methods

LA or vehicle was applied in two dry eye models: an in vitro hyperosmotic stress model and an in vivo desiccating stress (DS) murine model. The viability of human corneal epithelial cells (HCECs) was measured using a cell counting kit (CCK-8). Tear secretion was assessed using the phenol red cotton test. The tear break-up time (TBUT) was recorded using 0.1% liquid fluorescein sodium. Corneal epithelial permeability was evaluated through Oregon green dextran (OGD) staining. Conjunctival goblet cells were counted using periodic acid-Schiff (PAS) staining. Terminal deoxynucleotidyl transfer dUTP nick-end labeling (TUNEL) staining was used to quantify apoptotic cells in both models. The expression of Ki-67 was measured in HCECs in the cell model while that of matrix metalloproteinase (MMP)-3 and -9 was measured in the murine model through immunofluorescence staining. Real-time quantitative PCR (RT-qPCR) was performed to assess the expression of MMP-3 and MMP-9 in the corneal epithelium and NLRP3, ASC, Caspase-1, interleukin (IL)-1β, IL-18, and tumor necrosis factor (TNF)-α in the conjunctiva. The protein expression levels of NLRP3, ASC, Caspase-1, IL-1β, and IL-18 in the conjunctiva were assessed via Western blot

Results

In the in vitro model, treatment of HCECs with LA showed no toxicity, increased proliferation, and reduced apoptosis. In the murine model, compared to the control, LA significantly increased tear production and TBUT, improved OGD staining, and increased the number of goblet cells. Topical treatment of LA to mice provided decreased expression of MMP-3, MMP-9, TNF-α, and apoptotic corneal epithelium. Topical administration of LA also suppressed the NLRP3 inflammasome in the dry eye disease (DED) murine model by decreasing the expression of NLRP3, ASC, Caspase-1, IL-1β, and IL-18 in the conjunctiva.

Conclusion

Our findings support the safety and efficacy of LA in the treatment of DED. LA alleviated corneal epithelial damage and suppressed NLRP3 inflammasome-mediated immunity in the conjunctiva in a murine model of DED.

目的探讨linarin (LA)对实验性干眼模型的影响及其作用机制。方法将linarin或载药分别应用于离体高渗应激模型和体内干眼应激(DS)小鼠模型。使用细胞计数试剂盒(CCK-8)测定人角膜上皮细胞(HCECs)的活力。泪液分泌采用酚红棉试验。用0.1%液体荧光素钠记录泪液破裂时间。通过俄勒冈绿葡聚糖(OGD)染色评估角膜上皮通透性。结膜杯状细胞计数采用周期性酸-希夫(PAS)染色。采用末端脱氧核苷酸转移dUTP镍端标记(TUNEL)染色定量两种模型的凋亡细胞。采用免疫荧光染色法检测小鼠模型中基质金属蛋白酶(MMP)-3和-9的表达,同时检测细胞模型中HCECs中Ki-67的表达。采用实时荧光定量PCR (RT-qPCR)检测大鼠角膜上皮组织中MMP-3、MMP-9及结膜组织中NLRP3、ASC、Caspase-1、白细胞介素(IL)-1β、IL-18、肿瘤坏死因子(TNF)-α的表达情况。Western blotresult检测结膜内NLRP3、ASC、Caspase-1、IL-1β和IL-18蛋白表达水平。在体外模型中,LA治疗HCECs无毒性,增殖增加,细胞凋亡减少。在小鼠模型中,与对照组相比,LA显著增加泪液产量和TBUT,改善OGD染色,增加杯状细胞数量。局部给予小鼠LA可降低MMP-3、MMP-9、TNF-α的表达和角膜上皮细胞凋亡。局部给药LA还通过降低结膜中NLRP3、ASC、Caspase-1、IL-1β和IL-18的表达来抑制干眼病(DED)小鼠模型中的NLRP3炎性体。结论本研究结果支持LA治疗DED的安全性和有效性。在小鼠DED模型中,LA减轻了角膜上皮损伤,抑制了结膜NLRP3炎症小体介导的免疫。
{"title":"Linarin ameliorates innate inflammatory response in an experimental dry eye model via modulation of the NLRP3 inflammasome","authors":"Chen Mei ,&nbsp;Li Jie ,&nbsp;Peng Jun ,&nbsp;Huang Yu ,&nbsp;Ouyang Weijie ,&nbsp;Liu Xiaoqing ,&nbsp;Shen Zhibin ,&nbsp;Li Changdong ,&nbsp;Wang Yi ,&nbsp;Peng Qinghua","doi":"10.1016/j.dcmed.2021.03.006","DOIUrl":"https://doi.org/10.1016/j.dcmed.2021.03.006","url":null,"abstract":"<div><h3>Objective</h3><p>To investigate the effect and mechanism of linarin (LA) in an experimental dry eye model</p></div><div><h3>Methods</h3><p>LA or vehicle was applied in two dry eye models: an <em>in vitro</em> hyperosmotic stress model and an <em>in vivo</em> desiccating stress (DS) murine model. The viability of human corneal epithelial cells (HCECs) was measured using a cell counting kit (CCK-8). Tear secretion was assessed using the phenol red cotton test. The tear break-up time (TBUT) was recorded using 0.1% liquid fluorescein sodium. Corneal epithelial permeability was evaluated through Oregon green dextran (OGD) staining. Conjunctival goblet cells were counted using periodic acid-Schiff (PAS) staining. Terminal deoxynucleotidyl transfer dUTP nick-end labeling (TUNEL) staining was used to quantify apoptotic cells in both models. The expression of Ki-67 was measured in HCECs in the cell model while that of matrix metalloproteinase (MMP)-3 and -9 was measured in the murine model through immunofluorescence staining. Real-time quantitative PCR (RT-qPCR) was performed to assess the expression of MMP-3 and MMP-9 in the corneal epithelium and NLRP3, ASC, Caspase-1, interleukin (IL)-1<em>β</em>, IL-18, and tumor necrosis factor (TNF)-<em>α</em> in the conjunctiva. The protein expression levels of NLRP3, ASC, Caspase-1, IL-1<em>β</em>, and IL-18 in the conjunctiva were assessed via Western blot</p></div><div><h3>Results</h3><p>In the <em>in vitro</em> model, treatment of HCECs with LA showed no toxicity, increased proliferation, and reduced apoptosis. In the murine model, compared to the control, LA significantly increased tear production and TBUT, improved OGD staining, and increased the number of goblet cells. Topical treatment of LA to mice provided decreased expression of MMP-3, MMP-9, TNF-<em>α</em>, and apoptotic corneal epithelium. Topical administration of LA also suppressed the NLRP3 inflammasome in the dry eye disease (DED) murine model by decreasing the expression of NLRP3, ASC, Caspase-1, IL-1<em>β</em>, and IL-18 in the conjunctiva.</p></div><div><h3>Conclusion</h3><p>Our findings support the safety and efficacy of LA in the treatment of DED. LA alleviated corneal epithelial damage and suppressed NLRP3 inflammasome-mediated immunity in the conjunctiva in a murine model of DED.</p></div>","PeriodicalId":33578,"journal":{"name":"Digital Chinese Medicine","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.dcmed.2021.03.006","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91975150","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Relationship between syndrome elements and anterior communicating artery opening in patients with smptomatic severe carotid artery stenosis/occlusion 症状性重度颈动脉狭窄/闭塞患者证候要素与前交通动脉开口的关系
Q3 Medicine Pub Date : 2021-03-01 DOI: 10.1016/j.dcmed.2021.03.005
Zhen Fei , Meng Fanxing , Dou Jinjuan , Louis Lei Jin , Qiu Jiwen

Objective

To study the relationship between syndrome elements and anterior communicating artery (ACoA) opening in patients with symptomatic severe carotid artery stenosis/occlusion.

Methods

Thirty-six patients with symptomatic severe carotid stenosis/occlusion were collected, including 26 patients with cerebral infarction and 10 patients with transient ischemic attack (TIA). Syndrome elements at five time points were collected. Computer tomography angiography (CTA) combined with magenic resonance angiograp (MRA) was used to evaluate the primary collateral circulation, and the prognosis and syndrome elements were statistically analyzed according to whether the ACoA was open or not.

Results

The ACoA was open more in the primary collateral circulation among patients with symptomatic severe carotid stenosis/occlusion. There was a statistically significant difference in national institute of health stroke scale (NIHSS) score improvement and good prognosis [the modified rankin scale (mRS) ≤ 2] between the ACoA open group and the ACoA non-open group on the 90th day (P < 0.05). The proportion of patients with internal wind syndrome, blood stasis syndrome, Qi deficiency syndrome, and Yin deficiency syndrome in the ACoA non-open group was higher than that in the open group.

Conclusion

In the patients with severe carotid artery stenosis/ occlusion, the group with presence of anterior communicating artery had better prognosis. The syndrome elements are more complex in the group without the presence of anterior communicating artery. The proportion of Qi deficiency syndrome was positively correlated with the non-opening of anterior communicating artery. The imaging evaluation of collateral circulation can provide guidance for syndrome differentiation and treatment.

目的探讨有症状性颈动脉严重狭窄/闭塞患者证候要素与前交通动脉(ACoA)开口的关系。方法收集有症状的重度颈动脉狭窄/闭塞患者36例,其中脑梗死患者26例,短暂性脑缺血发作(TIA)患者10例。采集5个时点的证候要素。采用计算机断层血管造影(CTA)联合磁共振血管造影(MRA)评估初级侧支循环,并根据ACoA是否通畅进行预后及证候因素统计分析。结果有症状的颈动脉严重狭窄/闭塞患者的第一侧枝循环ACoA更开放。ACoA开放组与非ACoA开放组在第90天美国国立卫生研究院卒中量表(NIHSS)评分改善及良好预后[改良排名量表(mRS)≤2]方面差异有统计学意义(P <0.05)。ACoA未开封组内风证、血瘀证、气虚证、阴虚证患者比例高于开封组。结论颈动脉严重狭窄/闭塞患者,前交通动脉存在组预后较好。无前交通动脉组的综合征因素更为复杂。气虚证比例与前交通动脉不通畅呈正相关。侧枝循环影像学评价可为辨证论治提供指导。
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引用次数: 0
Study on GC-MS fingerprint of petroleum ether fraction of Shenqi Jiangtang Granules 参芪降糖颗粒石油醚组分的GC-MS指纹图谱研究
Q3 Medicine Pub Date : 2021-03-01 DOI: 10.1016/j.dcmed.2021.03.004
Li Bingbing , Wang Qian , Li Caixia , Huang Wenjing , Chen Guoliang , Guan Yongxia , Muhammad Ishaq , Xiao Xue , Yan Shikai

Objective

To establish gas chromatography-mass spectrometry (GC-MS) fingerprint method for the petroleum ether fraction of Shenqi Jiangtang Granules (SQJTG) and evaluate the product quality.

Methods

The GC-MS fingerprint of petroleum ether fraction of SQJTG was established by GC-MS, and the chemical components corresponding to the fingerprint peaks were structurally identified on NIST2014. The batch consistency of SQJTG products was evaluated based on the chemical composition of petroleum ether parts by using fingerprint similarity evaluation and Principal components analysis (PCA) technology. At the same time, Hotelling's T2 and DMODX statistics are used to set the control range for the quality of different batches of products.

Results

Twenty-two components were identified from the petroleum ether part of SQJTG, accounting for 60.94% of the total components separated. The similarity of fingerprints of petroleum ether parts of 24 batches of SQJTG was greater than 0.95. The PCA of 24 batches of samples were all under the control limits of Hotellin’s T2 and DMODX statistics, indicating that the petroleum ether parts of different batches of SQJTG were consistent.

Conclusion

The developed GC-MS fingerprint method can be used to evaluate the quality of SQJTG.

目的建立参芪降糖颗粒中石油醚组分的气相色谱-质谱(GC-MS)指纹图谱方法,并对产品质量进行评价。方法采用GC-MS建立SQJTG石油醚组分的GC-MS指纹图谱,并在NIST2014上对指纹图谱峰对应的化学成分进行结构鉴定。采用指纹相似度评价和主成分分析(PCA)技术,基于石油醚组分的化学成分对SQJTG产品的批次一致性进行了评价。同时,采用Hotelling的T2和DMODX统计,设定不同批次产品的质量控制范围。结果从SQJTG的石油醚部分共鉴定出22种组分,占总分离组分的60.94%。24批SQJTG的石油醚部分指纹图谱相似度均大于0.95。24批样品的PCA均在Hotellin的T2和DMODX统计量的控制范围内,说明不同批次SQJTG的石油醚部分是一致的。结论所建立的气相色谱-质谱指纹图谱法可用于评价黄芪多糖的质量。
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引用次数: 2
Artificial intelligence meets traditional Chinese medicine: a bridge to opening the magic box of sphygmopalpation for pulse pattern recognition 人工智能与中医相遇:打开脉象触诊魔盒的桥梁
Q3 Medicine Pub Date : 2021-03-01 DOI: 10.1016/j.dcmed.2021.03.001
Leung Yeuk-Lan Alice , Guan Binghe , Chen Shuang , Chan Hoyin , Kong Kawai , Li Wenjung , Shen Jiangang

<title/> Artificial intelligence (AI) aims to mimic human cognitive functions and execute intellectual activities like that performed by humans dealing with an uncertain environment. The rapid development of AI technology provides powerful tools to analyze massive amounts of data, facilitating physicians to make better clinical decisions or even replace human judgment in healthcare. Advanced AI technology also creates novel opportunities for exploring the scientific basis of traditional Chinese medicine (TCM) and developing the standardization and digitization of TCM pulse diagnostic methodology. In the present study, we review and discuss the potential application of AI technology in TCM pulse diagnosis. The major contents include the following aspects: (1) a brief introduction of the general concepts and knowledge of TCM pulse diagnosis or palpation, (2) landmark developments in AI technology and the applications of common AI deep learning algorithms in medical practice, (3) the current progress of AI technology in TCM pulse diagnosis, (4) challenges and perspectives of AI technology in TCM pulse diagnosis. In conclusion, the pairing of TCM with modern AI technology will bring novel insights into understanding the scientific principles underlying TCM pulse diagnosis and creating opportunities for the development of AI deep learning technology for the standardization and digitalization of TCM pulse diagnosis.

& lt;标题/比;人工智能(AI)旨在模仿人类的认知功能,并执行人类在处理不确定环境时所执行的智力活动。人工智能技术的快速发展为分析大量数据提供了强大的工具,帮助医生做出更好的临床决策,甚至在医疗保健中取代人类的判断。先进的人工智能技术也为探索中医的科学基础和发展中医脉诊方法的标准化和数字化创造了新的机会。在本研究中,我们回顾并讨论了人工智能技术在中医脉象诊断中的潜在应用。主要内容包括以下几个方面:(1)简要介绍中医脉诊或触诊的一般概念和知识;(2)人工智能技术的里程碑式发展以及常见的人工智能深度学习算法在医疗实践中的应用;(3)人工智能技术在中医脉诊中的当前进展;(4)人工智能技术在中医脉诊中的挑战和展望。总之,中医与现代人工智能技术的结合将为理解中医脉诊的科学原理带来新的见解,并为人工智能深度学习技术的发展创造机会,以实现中医脉诊的标准化和数字化。
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引用次数: 13
Detoxification of toxic herbs in TCM prescription based on modulation of efflux transporters 基于外排转运体调节的中药解毒研究
Q3 Medicine Pub Date : 2021-03-01 DOI: 10.1016/j.dcmed.2021.03.002
Qian Liyunhe , He Yufei , Zhang Mei , Xie Ying

Traditional Chinese medicines (TCMs) have been used to prevent and treat various diseases for thousands of years. Promoting efficacy and reducing toxicity by the compatibility theory of TCMs has attracted increasing attention, especially for the toxicity of herbs. Studies have pointed out the interactions between the active compounds of herbs and transporters in the detoxification process of toxic compounds. Here, we summarize data on five toxic herbs commonly used in TCMs and their related efflux transporters to reduce toxicity to offer a scientific rationale for the compatibility principle of TCMs and provide guidance for the rational clinical use of TCMs.

几千年来,人们一直用中药来预防和治疗各种疾病。中药配伍理论的增效降毒作用越来越受到人们的重视,尤其是对中草药的毒性研究。研究指出,在有毒物质解毒过程中,中草药的活性成分与转运体之间存在相互作用。本文通过对中药常用的五种有毒中草药及其相关外排转运体的数据进行总结,以降低毒性,为中药配伍原则提供科学依据,为临床合理使用中药提供指导。
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引用次数: 2
Physical Therapy Modalities of Western Medicine and Traditional Chinese Medicine for Meibomian Gland Dysfunction 中西医结合治疗睑板腺功能障碍的物理治疗方法
Q3 Medicine Pub Date : 2020-12-01 DOI: 10.1016/j.dcmed.2020.12.001
Li Jie , Ou Shang-Kun , Li Wei , Liu Zu-Guo , Peng Qing-Hua

The meibomian gland is a unique sebaceous gland located in the eyelid. Its main function is to secrete lipids and form the lipid layer of the tear film to delay the evaporation of waterborne tears, increase the surface tension of the tear film, and to lubricate the contact area of the eyelid and eyeball. Abnormal secretion of the meibomian gland is known as meibomian gland dysfunction (MGD), which has become the most important cause of evaporative dry eye disease (DED). The clinical pathophysio-logical process and underlying molecular mechanisms of MGD are not clear. As serious side effects may occur with the long-term use of hormonotherapy and non-steroidal anti-inflammatory drugs (NSAIDs) for the treatment of MGD, meibomian gland physiotherapy is considered the most effective and safest therapy for MGD. This review summarizes the physical therapy modalities of western medicine (WM) and traditiond Chinese medicine (TCM) for the treatment of MGD to provide optimal treatments for these patients and to further lay a foundation for mechanistic studies of MGD.

睑板腺是位于眼睑上的一种独特的皮脂腺。其主要作用是分泌脂质,形成泪膜的脂质层,延缓水性泪液的蒸发,增加泪膜的表面张力,润滑眼睑和眼球的接触区域。睑板腺分泌异常被称为睑板腺功能障碍(MGD),已成为蒸发性干眼病(DED)的重要病因。MGD的临床病理生理过程和潜在的分子机制尚不清楚。由于长期使用激素治疗和非甾体抗炎药(NSAIDs)治疗MGD可能会出现严重的副作用,因此睑板腺物理治疗被认为是MGD最有效和最安全的治疗方法。本文综述了西医和中医治疗MGD的物理治疗方式,以期为MGD患者提供最佳治疗方案,并进一步为MGD的机制研究奠定基础。
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引用次数: 2
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Digital Chinese Medicine
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