Therapeutic delivery最新文献

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Modeling and evaluation of ivermectin release kinetics from 3D-printed tablets. 三维打印片剂伊维菌素释放动力学的建模与评估。
IF 3
Therapeutic delivery Pub Date : 2024-01-01 Epub Date: 2024-10-16 DOI: 10.1080/20415990.2024.2412511
Cintia Alejandra Briones Nieva, Juan Pablo Real, Santiago Nicolás Campos, Analía Irma Romero, Mercedes Villegas, Elio Emilio Gonzo, José María Bermúdez, Santiago Daniel Palma, Alicia Graciela Cid
{"title":"Modeling and evaluation of ivermectin release kinetics from 3D-printed tablets.","authors":"Cintia Alejandra Briones Nieva, Juan Pablo Real, Santiago Nicolás Campos, Analía Irma Romero, Mercedes Villegas, Elio Emilio Gonzo, José María Bermúdez, Santiago Daniel Palma, Alicia Graciela Cid","doi":"10.1080/20415990.2024.2412511","DOIUrl":"10.1080/20415990.2024.2412511","url":null,"abstract":"<p><p><b>Aim:</b> This study focused on evaluating the influence of geometric dimensions on the drug release kinetics of 3D-printed tablets.<b>Materials & methods:</b> An ink based on Gelucire 50/13 was prepared to print ivermectin-loaded tablets. The ink was characterized physicochemically and tablet dissolution tests were carried out.<b>Results:</b> The results confirmed the suitability of the ink for 3D printing at a temperature >46°C. Changes in the crystallinity of ivermectin were observed without chemical interactions with the polymer. 3D printed tablets with varied proportional sizes showed dual behavior in their release profiles, while tablets with only thickness reduction exhibited zero-order kinetics.<b>Conclusion:</b> These findings highlight the versatility of 3D printing to create systems with specific and customized release profiles.</p>","PeriodicalId":22959,"journal":{"name":"Therapeutic delivery","volume":"15 11","pages":"845-858"},"PeriodicalIF":3.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11497972/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142475371","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: 0
Fabrication and evaluation of nanoemulsion based insulin loaded microneedles for transdermal drug delivery. 用于透皮给药的基于纳米乳液的胰岛素微针的制造和评估。
IF 3
Therapeutic delivery Pub Date : 2024-01-01 Epub Date: 2024-07-29 DOI: 10.1080/20415990.2024.2377065
Fatima Ramzan Ali, Muhammad Harris Shoaib, Syed Abid Ali, Rabia Ismail Yousuf, Farrukh Rafiq Ahmed, Fahad Siddiqui, Sana Sarfaraz, Rameez Raja
{"title":"Fabrication and evaluation of nanoemulsion based insulin loaded microneedles for transdermal drug delivery.","authors":"Fatima Ramzan Ali, Muhammad Harris Shoaib, Syed Abid Ali, Rabia Ismail Yousuf, Farrukh Rafiq Ahmed, Fahad Siddiqui, Sana Sarfaraz, Rameez Raja","doi":"10.1080/20415990.2024.2377065","DOIUrl":"10.1080/20415990.2024.2377065","url":null,"abstract":"<p><p><b>Aim:</b> Insulin therapy require self-administration of subcutaneous injection leading to painful and inconvenient drug therapy. The aim is to fabricate nanoemulsion (NE) based insulin loaded microneedles with improved bioavailability and patient compliance.<b>Materials & methods:</b> Different ratios of polyvinyl alcohol and polyvinylpyrrolidone as polymers were prepared through micro-molding technique for microneedles. Characterization of were performed using scanning electron microscope, differential scanning calorimetry, Fourier-transform infrared spectroscopy and circular dichroism. Mechanical strength, hygroscopicity and pain perception of these microneedles were also evaluated. <i>In vitro</i> release, permeation and <i>in vivo</i> PK/PD study of NE-based microneedles were conducted.<b>Results:</b> NE-based microneedles of insulin have improved bioavailability and quick response.<b>Conclusion:</b> Microneedles loaded with insulin can be effectively delivered insulin transdermally to treat diabetes with increased convenience and patient compliance.</p>","PeriodicalId":22959,"journal":{"name":"Therapeutic delivery","volume":" ","pages":"605-617"},"PeriodicalIF":3.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11412143/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141789108","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: 0
January 2024 industry update. 2024 年 1 月行业更新。
IF 3
Therapeutic delivery Pub Date : 2024-01-01 Epub Date: 2024-05-09 DOI: 10.1080/20415990.2024.2346045
Patrick Lim, Nebojsa Stilinovic, Armin Mooranian, Hani Al-Salami
{"title":"January 2024 industry update.","authors":"Patrick Lim, Nebojsa Stilinovic, Armin Mooranian, Hani Al-Salami","doi":"10.1080/20415990.2024.2346045","DOIUrl":"https://doi.org/10.1080/20415990.2024.2346045","url":null,"abstract":"","PeriodicalId":22959,"journal":{"name":"Therapeutic delivery","volume":"15 6","pages":"393-398"},"PeriodicalIF":3.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141856625","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A novel liposomal formulation for ocular delivery of caspofungin: an experimental study by quality by design-based approach. 一种用于眼部给药卡泊芬净的新型脂质体配方:基于设计质量方法的实验研究。
IF 3
Therapeutic delivery Pub Date : 2024-01-01 Epub Date: 2024-08-05 DOI: 10.1080/20415990.2024.2379756
Mercy Macwan, Himanshu Paliwal, Bhupendra G Prajapati
{"title":"A novel liposomal formulation for ocular delivery of caspofungin: an experimental study by quality by design-based approach.","authors":"Mercy Macwan, Himanshu Paliwal, Bhupendra G Prajapati","doi":"10.1080/20415990.2024.2379756","DOIUrl":"10.1080/20415990.2024.2379756","url":null,"abstract":"<p><p><b>Aim:</b> This study focuses on the development of a Caspofungin liposome for efficient ocular delivery by enhancing corneal penetration.<b>Method:</b> Quality by design (QbD) approach was adopted to identify critical factors that influence final liposomal formulation. The liposome developed using thin film hydration after optimization was subjected to characterization for physicochemical properties, irritation potential and corneal uptake.<b>Results:</b> The numerical optimization suggests an optimal formulation with a desirability value of 0.706, using CQAs as optimization goals with 95% prediction intervals. The optimized formulation showed no signs of irritation potential along with observation of significant corneal permeation.<b>Conclusion:</b> The liposomal formulation increased the permeability of Caspofungin, which could enhance the efficacy for the treatment of conditions, like fungal keratitis.</p>","PeriodicalId":22959,"journal":{"name":"Therapeutic delivery","volume":" ","pages":"667-683"},"PeriodicalIF":3.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11415022/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141890136","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: 0
Dual combination of resveratrol and pterostilbene aqueous core nanocapsules for integrated prostate cancer targeting. 白藜芦醇和紫檀素水芯纳米胶囊的双重组合,用于前列腺癌的综合靶向治疗。
IF 3
Therapeutic delivery Pub Date : 2024-01-01 Epub Date: 2024-08-12 DOI: 10.1080/20415990.2024.2380239
Alok Nath Sharma, Prabhat Kumar Upadhyay, Hitesh Kumar Dewangan
{"title":"Dual combination of resveratrol and pterostilbene aqueous core nanocapsules for integrated prostate cancer targeting.","authors":"Alok Nath Sharma, Prabhat Kumar Upadhyay, Hitesh Kumar Dewangan","doi":"10.1080/20415990.2024.2380239","DOIUrl":"10.1080/20415990.2024.2380239","url":null,"abstract":"<p><p><b>Aim:</b> Development and evaluation of aqueous core nanocapsules (ACNs) of BCS-II-class drug like resveratrol (RSV) and pterostilbene (PTE) for prostate cancer.<b>Materials & methods:</b> Identify synergistic effects of molar ratios of RSV and PTE against PC-3 cell. Selected ratio of drugs was added to ACNs by double-emulsification-method using Box-Behnken design. Further, assessed for physicochemical characterization, release kinetics, compatibility, <i>in vitro</i> cytotoxicity, <i>in vivo</i> pharmacokinetic and biodistribution studies.<b>Results:</b> Selected 1:1 ratio of RSV and PTE had greatest synergy potential have smaller particle-size (128.1 ± 3.21 nm), zeta-potential (-22.12 ± 0.2 mV), 0.53 PDI, improved encapsulation (87% for RSV, 72% for PTE), stable, no systemic toxicity, high biodistributed/accumulated in prostate cells.<b>Conclusion:</b> ACNs exhibited high t<sub>1/2</sub> (12.42 ± 1.92 hs) and 8.20 ± 8.21 hs Mean Residence Time and lower clearance, proving the high effectiveness for prostate cancer.</p>","PeriodicalId":22959,"journal":{"name":"Therapeutic delivery","volume":" ","pages":"685-698"},"PeriodicalIF":3.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11415016/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141917480","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: 0
Therapeutic Delivery - Industry Update covering February 2024. 治疗传递--2024 年 2 月行业更新。
IF 3
Therapeutic delivery Pub Date : 2024-01-01 Epub Date: 2024-09-03 DOI: 10.1080/20415990.2024.2365614
Iain Simpson
{"title":"Therapeutic Delivery - Industry Update covering February 2024.","authors":"Iain Simpson","doi":"10.1080/20415990.2024.2365614","DOIUrl":"10.1080/20415990.2024.2365614","url":null,"abstract":"","PeriodicalId":22959,"journal":{"name":"Therapeutic delivery","volume":" ","pages":"481-488"},"PeriodicalIF":3.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142120671","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Artemisinin emulgel ameliorates cartilage degradation in knee osteoarthritis: in vitro and in vivo studies. 青蒿素凝胶改善膝关节骨关节炎软骨退化:体外和体内研究
IF 3
Therapeutic delivery Pub Date : 2024-01-01 Epub Date: 2024-11-06 DOI: 10.1080/20415990.2024.2418281
Samiksha Thote, Atul Mourya, Shristi Arya, Hoshiyar Singh, Prashanth Kumar, Santosh Kumar Guru, Jitender Madan
{"title":"Artemisinin emulgel ameliorates cartilage degradation in knee osteoarthritis: <i>in vitro</i> and <i>in vivo</i> studies.","authors":"Samiksha Thote, Atul Mourya, Shristi Arya, Hoshiyar Singh, Prashanth Kumar, Santosh Kumar Guru, Jitender Madan","doi":"10.1080/20415990.2024.2418281","DOIUrl":"10.1080/20415990.2024.2418281","url":null,"abstract":"<p><p><b>Aim:</b> Laboratory scale-up of artemisinin-loaded emulgel (ART-emulgel) was carried out and characterized for therapeutic performance in osteoarthritis (OA).<b>Materials & methods:</b> The solubility of ART in various oils, surfactants and co-surfactants were screened for construction of pseudo ternary phase diagram (TPD), followed by scale-up of artemisinin loaded nanoemulsion (ART-NE). ART-NE was amalgamated with Carbopol Ultrez 10-NF to prepare ART-emulgel that was later characterized <i>in vitro</i> and <i>in vivo</i> to analyze therapeutic efficacy in monosodium-iodoacetate (MIA) induced knee OA.<b>Results:</b> The droplet diameter of ART-NE was estimated to be 104.3 ± 2.593 nm with a polydispersity index of 0.245 ± 0.019 in addition to ζ-potential of 0.434 ± 0.028 mV. Steady-state flux and permeability coefficient for ART-emulgel were estimated to be 0.651 ± 0.031 µg.cm<sup>2</sup>/h and 0.245 ± 0.011 cm/h, respectively. ART-emulgel demonstrated 43.18% reduction in COX-2 level; 52.28% drop in IL-1β, and 88.78% alleviation of Tumor Necrosis Factor-α (TNF-α) level when compared with monosodium-iodoacetate induced OA rats. ART-emulgel and injectable ART (intra-articular; I.A) portrayed minor synovial erosion compared with blank and diclofenac emulgel. Histopathological evidences indicated restoration of cartilage integrity followed by reduction of OARSI scores in ART-emulgel when compared with disease control animals.<b>Conclusion:</b> ART-emulgel is a potential dosage form for translating into a clinically viable product for the management of OA.</p>","PeriodicalId":22959,"journal":{"name":"Therapeutic delivery","volume":" ","pages":"939-955"},"PeriodicalIF":3.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11583592/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142582738","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: 0
Sodium alginate/carboxymethylcellulose gel formulations containing Capparis sepieria plant extract for wound healing. 海藻酸钠/羧甲基纤维素凝胶配方,含用于伤口愈合的蓝花楹植物提取物。
IF 3
Therapeutic delivery Pub Date : 2024-01-01 Epub Date: 2024-11-12 DOI: 10.1080/20415990.2024.2418800
Sindi P Ndlovu, Shirley C M Motaung, Samson A Adeyemi, Philemon Ubanako, Lindokuhle M Ngema, Thierry Youmbi Fonkui, Derek Tantoh Ndinteh, Pradeep Kumar, Yahya E Choonara, Blessing A Aderibigbe
{"title":"Sodium alginate/carboxymethylcellulose gel formulations containing <i>Capparis sepieria</i> plant extract for wound healing.","authors":"Sindi P Ndlovu, Shirley C M Motaung, Samson A Adeyemi, Philemon Ubanako, Lindokuhle M Ngema, Thierry Youmbi Fonkui, Derek Tantoh Ndinteh, Pradeep Kumar, Yahya E Choonara, Blessing A Aderibigbe","doi":"10.1080/20415990.2024.2418800","DOIUrl":"10.1080/20415990.2024.2418800","url":null,"abstract":"<p><p><b>Aim:</b> Using appropriate wound dressings is crucial when treating burn wounds to promote accelerated healing.<b>Materials & methods:</b> Sodium alginate (SA)-based gels containing Carboxymethyl cellulose (CMC) and Pluronic F127 were prepared. The formulations. SA/CMC/Carbopol and SA/CMC/PluronicF127 were loaded with aqueous root extract of <i>Capparis sepiaria</i>. The formulations were characterized using appropriate techniques.<b>Results:</b> The gels' viscosity was in the range of 676.33 ± 121.76 to 20.00 ± 9.78 cP and <i>in vitro</i> whole blood kinetics showed their capability to induce a faster clotting rate. They also supported high cell viability of 80% with cellular migration and proliferation. Their antibacterial activity was significant against most bacteria strains used in the study.<b>Conclusion:</b> The gels' distinct features reveal their potential application as wound dressings for burn wounds.</p>","PeriodicalId":22959,"journal":{"name":"Therapeutic delivery","volume":" ","pages":"921-937"},"PeriodicalIF":3.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11583625/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142628741","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: 0
Exploring delivery systems for targeted nanotechnology-based gene therapy in the inner ear. 探索基于纳米技术的内耳靶向基因治疗输送系统。
IF 3
Therapeutic delivery Pub Date : 2024-01-01 Epub Date: 2024-09-26 DOI: 10.1080/20415990.2024.2389032
Thomas Foster, Patrick Lim, Corina Mihaela Ionescu, Susbin Raj Wagle, Bozica Kovacevic, Armin Mooranian, Hani Al-Salami
{"title":"Exploring delivery systems for targeted nanotechnology-based gene therapy in the inner ear.","authors":"Thomas Foster, Patrick Lim, Corina Mihaela Ionescu, Susbin Raj Wagle, Bozica Kovacevic, Armin Mooranian, Hani Al-Salami","doi":"10.1080/20415990.2024.2389032","DOIUrl":"10.1080/20415990.2024.2389032","url":null,"abstract":"<p><p>Hearing loss places a significant burden on our aging population. However, there has only been limited progress in developing therapeutic techniques to effectively mediate this condition. This review will outline several of the most commonly utilized practices for the treatment of sensorineural hearing loss before exploring more novel techniques currently being investigated via both <i>in vitro</i> and <i>in vivo</i> research. This review will place particular emphasis on novel gene-delivery technologies. Primarily, it will focus on techniques used to deliver genes that have been shown to encourage the proliferation and differentiation of sensory cells within the inner ear and how these technologies may be translated into providing clinically useful results for patients.</p>","PeriodicalId":22959,"journal":{"name":"Therapeutic delivery","volume":" ","pages":"801-818"},"PeriodicalIF":3.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11457609/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142354279","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: 0
Enhancing Rose Bengal penetration in ex vivo human corneas using iontophoresis. 利用离子透入技术提高罗斯孟加拉红在体外人类角膜中的渗透率。
IF 3
Therapeutic delivery Pub Date : 2024-01-01 Epub Date: 2024-07-18 DOI: 10.1080/20415990.2024.2371778
James M Lai, Justin Chen, Juan Carlos Navia, Heather Durkee, Alex Gonzalez, Cornelis Rowaan, Timothy Arcari, Mariela C Aguilar, Katrina Llanes, Noel Ziebarth, Jaime D Martinez, Darlene Miller, Harry W Flynn, Guillermo Amescua, Jean-Marie Parel
{"title":"Enhancing Rose Bengal penetration in <i>ex vivo</i> human corneas using iontophoresis.","authors":"James M Lai, Justin Chen, Juan Carlos Navia, Heather Durkee, Alex Gonzalez, Cornelis Rowaan, Timothy Arcari, Mariela C Aguilar, Katrina Llanes, Noel Ziebarth, Jaime D Martinez, Darlene Miller, Harry W Flynn, Guillermo Amescua, Jean-Marie Parel","doi":"10.1080/20415990.2024.2371778","DOIUrl":"10.1080/20415990.2024.2371778","url":null,"abstract":"<p><p><b>Aim:</b> Rose Bengal photodynamic antimicrobial therapy (RB-PDAT) has poor corneal penetration, limiting its efficacy against acanthamoeba keratitis (AK). Iontophoresis enhances corneal permeation of charged molecules, piquing interest in its effects on RB in <i>ex vivo</i> human corneas.<b>Methods:</b> Five donor whole globes each underwent iontophoresis with RB, soaking in RB, or were soaked in normal saline (controls). RB penetration and corneal thickness was assessed using confocal microscopy.<b>Results:</b> Iontophoresis increased RB penetration compared with soaking (177 ± 9.5 μm vs. 100 ± 5.7 μm, <i>p</i> < 0.001), with no significant differences in corneal thickness between groups (460 ± 87 μm vs. 407 ± 69 μm, <i>p</i> = 0.432).<b>Conclusion:</b> Iontophoresis significantly improves RB penetration and its use in PDAT could offer a novel therapy for acanthamoeba keratitis. Further studies are needed to validate clinical efficacy.</p>","PeriodicalId":22959,"journal":{"name":"Therapeutic delivery","volume":" ","pages":"567-575"},"PeriodicalIF":3.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11412146/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141634581","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: 0
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