Technology Readiness Level Roadmap for Developing Innovative Herbal Medicinal Products

被引:1
|
作者
Pagani, Eduardo [1 ,2 ]
Ropke, Cristina Dislich [2 ]
Soares, Cristiane Mota [3 ]
Perez, Sandra Aurora Chavez [3 ]
Benevides, Paulo Jose Coelho [4 ]
Barbosa, Barbara Sena [2 ]
Carvalho, Ana Cecilia Bezerra [5 ]
Behrens, Maria Dutra [6 ]
机构
[1] Azidus Brasil, Med Dept, BR-13271130 Valinhos, SP, Brazil
[2] Centroflora Grp, Innovat Dept, BR-06460040 Campinas, SP, Brazil
[3] Fundacao Oswaldo Cruz, Inst Drug Technol Farmanguinhos, Project Management Off, Vice Direct Educ Res & Innovat, BR-21041250 Rio De Janeiro, RJ, Brazil
[4] Fundacao Oswaldo Cruz, Business Off, BR-79081746 Campo Grande, MS, Brazil
[5] Brazilian Hlth Regulatory Agcy, Agencia Nacl Vigilancia Sanit ANVISA, GMESP, Brasilia, DF, Brazil
[6] Oswaldo Cruz Fdn FIOCRUZ, Inst Pharmaceut Technol, Dept Nat Prod, Vice Direct Educ Res & Innovat, BR-21041250 Rio De Janeiro, RJ, Brazil
关键词
phytotherapy; technology readiness level; herbal substance; herbal preparation; herbal medicinal products; drug discovery; drug development; NATURAL-PRODUCTS; DRUG DISCOVERY; ASSESSMENTS; RELEVANT;
D O I
10.3390/ph17060703
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Despite the vast global botanical diversity, the pharmaceutical development of herbal medicinal products (HMPs) remains underexploited. Of over 370,000 described plant species, only a few hundred are utilized in HMPs. Most of these have originated from traditional use, and only a minority come from megadiverse countries. Exploiting the pharmacological synergies of the hundreds of compounds found in poorly studied plant species may unlock new therapeutic possibilities, enhance megadiverse countries' scientific and socio-economic development, and help conserve biodiversity. However, extensive constraints in the development process of HMPs pose significant barriers to transforming this unsatisfactory socio-economic landscape. This paper proposes a roadmap to overcome these challenges, based on the technology readiness levels (TRLs) introduced by NASA to assess the maturity of technologies. It aims to assist research entities, manufacturers, and funding agencies from megadiverse countries in the discovery, development, and global market authorization of innovative HMPs that comply with regulatory standards from ANVISA, EMA, and FDA, as well as WHO and ICH guidelines.
引用
收藏
页数:23
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