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Patent highlights June - July 2024. 专利亮点2024年6月- 7月。
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-03-07 DOI: 10.1080/20468954.2025.2459586
Hermann A M Mucke

A snapshot of noteworthy recent developments in the patent literature of relevance to pharmaceutical and medical research and development.

与制药和医学研究与开发相关的专利文献中值得注意的最新发展概况。
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引用次数: 0
Patent highlights August-September 2023. 2023 年 8 月至 9 月的专利要点。
IF 1.3 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-03-18 DOI: 10.4155/ppa-2023-0039
Hermann Am Mucke

A snapshot of noteworthy recent developments in the patent literature of relevance to pharmaceutical and medical research and development.

与制药和医疗研发相关的专利文献中值得关注的最新进展快照。
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引用次数: 0
Patent Highlights June-July 2023. 2023 年 6 月至 7 月的专利亮点。
IF 1.3 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-03-18 DOI: 10.4155/ppa-2023-0035
Hermann Am Mucke

A snapshot of noteworthy recent developments in the patent literature of relevance to pharmaceutical and medical research and development.

与制药和医疗研发相关的专利文献中值得关注的最新进展快照。
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引用次数: 0
Emerging patents versus brain eating amoebae, Naegleria fowleri. 新兴专利与吃脑变形虫,福氏奈格里亚。
IF 2.1 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-01-01 Epub Date: 2025-02-03 DOI: 10.1080/20468954.2025.2459584
Ruqaiyyah Siddiqui, David Lloyd, Naveed Ahmed Khan

Primary Amoebic Meningoencephalitis (PAM) is a severe and often fatal infection caused by the free-living amoebae Naegleria fowleri. This condition typically results from exposure to contaminated warm freshwater/inadequately treated recreational water/or ablution/nasal irrigation with contaminated water. The management of PAM is hindered by the absence of effective treatment coupled with challenges in early diagnosis. This review explores emerging patents that could be utilized for the treatment, diagnosis of PAM, as well as water treatment. Recent patents from the past five years, along with research and innovations are reviewed and categorized into therapeutic agents, water treatment technologies, and diagnostic methods. It is hoped that collaboration and awareness between pharmaceutical companies, water industries, and academic institutions is essential for advancing effective strategies against this severe central nervous system pathogen.

原发性阿米巴脑膜脑炎(PAM)是由自由生活的福氏纳格里阿米巴原虫引起的一种严重且往往致命的感染。这种情况通常是由于暴露于受污染的温暖淡水/未经充分处理的娱乐用水/或用受污染的水洗澡/鼻腔冲洗造成的。由于缺乏有效的治疗和早期诊断方面的挑战,PAM的管理受到阻碍。本文综述了可用于PAM治疗、诊断以及水处理的新兴专利。最近的专利从过去的五年,随着研究和创新进行审查,并分类为治疗剂,水处理技术和诊断方法。希望制药公司、水工业和学术机构之间的合作和认识对于推进对抗这种严重中枢神经系统病原体的有效战略至关重要。
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引用次数: 0
Developments in research and commercialization of PI3K and AKT targets: a patent-based landscape. PI3K和AKT靶点的研究和商业化进展:基于专利的前景。
IF 2.1 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-01-01 Epub Date: 2025-02-24 DOI: 10.1080/20468954.2025.2470102
Hai-Long Zhang, Zhaochen Lin, Ying Zhang

PI3K and AKT signaling pathway has been linked to the pathophysiology of various diseases. This pathway has emerged as a crucial therapeutic strategy for cancer and other diseases. To better understand recent development of PI3K and AKT, a patent-based landscape study was performed. The results shows that both PI3K and AKT targets have shown prolific patent filings over the past 20 years. This study is the first to depict the therapeutic applications of both PI3K and AKT targets based on a patent big data analysis. Ten key therapeutic applications were identified, with over 77% of patents related to anti-cancer therapy for both PI3K and AKT targets. Additionally, our findings show that combination therapy is a distinguishing feature for drugs targeting both PI3K and AKT. The average time from patent application to drug approval for PI3K target drugs is 8.8 years. PI3K target drugs obtain market approval faster compared to AKT drugs. Approximately, 2 years of patent term extension could be obtained if the time from the patent application date to the drug approval date is less than 10 years.

PI3K和AKT信号通路与多种疾病的病理生理有关。这种途径已经成为癌症和其他疾病的关键治疗策略。为了更好地了解PI3K和AKT的最新进展,我们进行了一项基于专利的景观研究。结果表明,PI3K和AKT靶点在过去20年中都有大量的专利申请。该研究首次基于专利大数据分析描述了PI3K和AKT靶点的治疗应用。确定了10个关键的治疗应用,超过77%的专利与针对PI3K和AKT靶点的抗癌治疗相关。此外,我们的研究结果表明,联合治疗是针对PI3K和AKT的药物的显著特征。PI3K靶标药物从专利申请到获批平均耗时8.8年。与AKT药物相比,PI3K靶向药物获得市场批准的速度更快。如果从专利申请日到药品批准日少于10年,大约可以获得2年的专利期限延长。
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引用次数: 0
Insights to the emerging potential of glucokinase activators as antidiabetic agent. 洞察葡萄糖激酶激活剂作为抗糖尿病药物的新兴潜力。
IF 2.1 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-01-01 Epub Date: 2024-09-11 DOI: 10.1080/20468954.2024.2389762
Anuradha Mehra, Shubham Kumar, Anu Mittal, Ruchi Kohli, Amit Mittal

The glucokinase enzyme (belongs to the hexokinase family) is present in liver cells and β-cells of the pancreas. Glucokinase acts as a catalyst in the conversion of glucose-6-phosphate from glucose which is rate-limiting step in glucose metabolism. Glucokinase becomes malfunctional or remains inactivated in diabetes. Glucokinase activators are compounds that bind at the allosteric site of the glucokinase enzyme and activate it. This article highlights the patent and recent research papers history with possible SAR from year 2014-2023. The data comprises the discussion of novel chemotypes (GKAs) that are being targeted for drug development and entered into clinical trials. GK activators have attracted massive interest since successful results have been reported from clinical trials data.

葡萄糖激酶(属于己糖激酶家族)存在于肝细胞和胰腺的β细胞中。葡萄糖激酶在从葡萄糖转化为 6-磷酸葡萄糖的过程中充当催化剂,这是葡萄糖代谢的限速步骤。糖尿病患者体内的葡萄糖激酶功能失常或失活。葡萄糖激酶激活剂是一种能与葡萄糖激酶的异构位点结合并激活它的化合物。本文重点介绍了2014-2023年的专利和最新研究论文历史,以及可能的SAR。这些数据包括对正在作为药物开发目标并进入临床试验的新型化学类型(GKA)的讨论。由于临床试验数据已报告了成功结果,GK 激活剂引起了广泛关注。
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引用次数: 0
Trivalent bispecific anti-MSLN2/CD3 antibody for cancer treatment. 肿瘤治疗用三价双特异性抗msln2 /CD3抗体。
IF 2.1 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-01-01 Epub Date: 2025-07-22 DOI: 10.1080/20468954.2025.2535939
Jorge Antonio Perez Saldaña, Donaciano Flores-Robles, Antonio Celestino Montes, Alejandro Millán-Vega, Pavel Sierra-Martínez, Martin Perez-Santos

Introduction: Mesothelin protein is an overexpressed molecule in epithelioid mesothelioma, epithelial ovarian cancer, and pancreatic adenocarcinoma, which is why it is considered a potential therapeutic target.

Areas covered: WO2024082060 patent describes a trivalent bispecific antibody directed against MSLN/CD3/MSLN, and lung cancer treatment method. This antibody exhibits binding activity to MSLN-containing tumor cells, as well as inhibition of tumor growth rate in murine models of lung and ovarian cancer.

Expert opinion: The trispecific structure suggesting that this antibody is a potential candidate for clinical trials for the treatment of lung cancer associated with high levels of MSLN expression.

间皮素蛋白是上皮样间皮瘤、上皮性卵巢癌和胰腺腺癌中过表达的分子,这就是为什么它被认为是一个潜在的治疗靶点。涉及领域:WO2024082060专利描述了一种针对MSLN/CD3/MSLN的三价双特异性抗体,以及肺癌治疗方法。该抗体对含有msln的肿瘤细胞具有结合活性,并在小鼠肺癌和卵巢癌模型中抑制肿瘤生长速率。专家意见:三特异性结构表明该抗体是临床试验中治疗与高水平MSLN表达相关的肺癌的潜在候选者。
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引用次数: 0
Patent highlights April-May 2024. 专利亮点2024年4 - 5月。
IF 2.1 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-01-01 Epub Date: 2025-02-11 DOI: 10.1080/20468954.2025.2459593
Hermann A M Mucke

A snapshot of noteworthy recent developments in the patent literature of relevance to pharmaceutical and medical research and development.

与制药和医学研究与开发相关的专利文献中值得注意的最新发展概况。
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引用次数: 0
Patent highlights December 2023-January 2024. 专利亮点2023年12月至2024年1月。
IF 2.1 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-01-01 Epub Date: 2024-09-04 DOI: 10.1080/20468954.2024.2390353
Hermann Am Mucke

A snapshot of noteworthy recent developments in the patent literature of relevance to pharmaceutical and medical research and development.

与制药和医学研究与开发相关的专利文献中值得注意的最新发展概况。
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引用次数: 0
3D-printed immediate release solid dosage forms: a patent evaluation of US11622940B2. 三维打印速释固体制剂:US11622940B2 的专利评估。
IF 2.1 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-01-01 Epub Date: 2024-09-04 DOI: 10.1080/20468954.2024.2389774
Akshay Sharma, Ritu Rathi, Sanchay Sharma, Tanikan Sangnim, Kampanart Huanbutta, Inderbir Singh

Three-dimensional (3D) printing is one of the most flexible technologies for preparing tablets, offering controlled drug release profiles. The current patent describes the preparation of immediate-release 3D-printed tablets of hydrochlorothiazide to improve disintegration and dissolution profile. The patent involves the preparation of drug-loaded filament via hot-melt extrusion and utilizing the same filaments for printing 3D-printed tablets using fused deposition modeling. The tablets were printed with different shapes and sizes by incorporating channels within the tablet spaces, termed as gaplets. The introduction of channels within the tablet design improves the disintegration and dissolution profile of the drug significantly. The morphological characteristic of 3D-printed tablets was studied by using scanning electron microscopy and revealed the presence of gaplets in the tablets.

三维(3D)打印是制备片剂最灵活的技术之一,可提供可控的药物释放曲线。目前的专利描述了氢氯噻嗪速释三维打印片剂的制备,以改善崩解和溶解曲线。该专利涉及通过热熔挤出法制备载药长丝,并利用熔融沉积建模技术将相同的长丝用于打印 3D 打印药片。通过在片剂空间中加入通道(称为小间隙),打印出不同形状和大小的片剂。在片剂设计中引入通道可显著改善药物的崩解和溶解曲线。使用扫描电子显微镜研究了 3D 打印片剂的形态特征,发现片剂中存在小间隙。
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引用次数: 0
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