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纳米生物技术领域的专利:跨辖区研究方法

Patents in Nanobiotechnology: A Cross Jurisdictional Approach.

作者信息

Manchikanti Padmavati, Uppala Shailaja, Bonta Ramesh Kumar

机构信息

Rajiv Gandhi School of IP Law, IIT Kharagpur, Kharagpur-721302, West Bengal. India.

出版信息

Recent Pat Biotechnol. 2017;11(1):52-70. doi: 10.2174/1872208310666161123100223.

Abstract

BACKGROUND

Bionanomaterials create new opportunities for advancing medical sciences and diseases treatment in relation to human health care. Innovations in the use of such nanomaterials and nanodevices can lead to significant improvements in the use of drugs/devices.

OBJECTIVE

The present study attempts to analyse patenting trends in different areas and compare the patentability criteria and the disclosure norms for nanobiotechnology inventions in countries such as US, EU and India in the field of diagnostics and therapeutics.

METHOD

Nanobiotechnology patents were identified based on the search using IPC/CPC as well as keywords conducted on Relecura (a web-based patent and portfolio analysis platform). Growth of filing/ grants and by area was analysed. Comparative analysis of the patentability criteria was done to identify challenges in prosecution of nanobiotechnology applications.

RESULT

US, China, followed by Europe are top patent filing countries in nanobiotechnology. Topic maps indicate medicinal preparations to be the major area of patenting. There is an increase in patenting in BRIC since 2000. The assessment of novelty, inventive step and specific disclosure norms in different jurisdictions related to nanobiotechnology inventions reveal challenges in patent prosecution.

CONCLUSION

79% of the overall nanobiotechnology patents are from the medicinal preparation area followed by a significant number in case of diagnostic and surgical applications. The upward trend in patenting indicates to the potential of inventions in the field of diagnostics. The development of objective and subjective criteria with respect to patentability indicates to elaborate patent office practice and prosecution in this area.

摘要

背景

生物纳米材料为推进医学科学及与人类医疗保健相关的疾病治疗创造了新机遇。此类纳米材料和纳米装置使用方面的创新能够显著改善药物/装置的应用。

目的

本研究试图分析不同领域的专利申请趋势,并比较美国、欧盟和印度等国家在诊断和治疗领域纳米生物技术发明的可专利性标准及公开规范。

方法

基于使用国际专利分类号/合作专利分类号以及在Relecura(一个基于网络的专利和组合分析平台)上进行的关键词搜索来识别纳米生物技术专利。分析了申请/授权数量的增长情况及按领域的增长情况。对可专利性标准进行了比较分析,以确定纳米生物技术应用审查中的挑战。

结果

美国、中国,其次是欧洲,是纳米生物技术领域专利申请最多的国家。主题地图显示药物制剂是主要的专利领域。自2000年以来,金砖国家的专利申请有所增加。对与纳米生物技术发明相关的不同司法管辖区的新颖性、创造性步骤和具体公开规范的评估揭示了专利审查中的挑战。

结论

总体纳米生物技术专利的79%来自药物制剂领域,其次是诊断和外科应用领域的大量专利。专利申请的上升趋势表明诊断领域发明的潜力。关于可专利性的客观和主观标准的制定表明该领域专利局的实践和审查工作较为精细。

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