大麻二酚(CBD)在脑区域和血浆鼻内给药CBD纳米制剂后的定量。

IF 4.3 Q1 PHARMACOLOGY & PHARMACY
Gunjan Upadhyay, Oksana Fihurka, Pranav Patel, Juan Sanchez-Ramos
{"title":"大麻二酚(CBD)在脑区域和血浆鼻内给药CBD纳米制剂后的定量。","authors":"Gunjan Upadhyay, Oksana Fihurka, Pranav Patel, Juan Sanchez-Ramos","doi":"10.1186/s42238-025-00308-5","DOIUrl":null,"url":null,"abstract":"<p><strong>Background and objective: </strong>Delivering therapeutic drugs to the brain for neurological disorders remains challenging due to the restrictive nature of the blood-brain barrier (BBB). Intranasal (IN) nanoparticle delivery may enhance the bioavailability of lipophilic cannabidiol (CBD), addressing limitations associated with systemic administration.</p><p><strong>Methods: </strong>Further optimization of nanoparticle properties is necessary to enhance brain uptake and therapeutic potential for neurological disorders. Following IN administration of the nanoformulation, C57BL/6 male mice (3-6 months old, n = 4/group) were euthanized at 2, 4, and 8 h. Plasma, olfactory bulb (OB), hippocampus (HP), striatum (STR), and cortex (CTX) were collected and analyzed for CBD and 7-COOH-CBD using liquid chromatography-mass spectrometry (LC-MS). Two-way analysis of variance with Tukey's multiple comparisons was used for statistical analysis.</p><p><strong>Results: </strong>CBD levels in the brain peaked at 4 h (5788 ng/mg), while 7-COOH-CBD reached its highest concentration at 2 h (3080 ng/mg). In plasma, maximum CBD levels were detected at 4 h (797 µg/mL), whereas 7-COOH-CBD peaked at 2 h (893 µg/mL). Despite measurable brain penetration, only 0.12% of the administered dose reached brain tissue, with 15.94% retained in plasma.</p><p><strong>Conclusion: </strong>This is the first study to provide the quantification of CBD and its 7CBD-COOH in various brain regions following IN administration of a CBD nanoformulation. While the approach facilitated brain delivery, overall bioavailability remained low. The use of four mice per group is a limitation that may impact the internal validity of these findings. This study aimed to develop a novel hydrophilic CBD nanoformulation for IN delivery and quantify its distribution and its major metabolite, 7-carboxy-cannabidiol (7CBD-COOH) in distinct brain regions and in plasma of mice.This methodology has the potential to overcome the limits of conventional CBD administration, providing a more effective treatment strategy for targeting brain diseases.</p>","PeriodicalId":101310,"journal":{"name":"Journal of cannabis research","volume":"7 1","pages":"63"},"PeriodicalIF":4.3000,"publicationDate":"2025-08-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12372218/pdf/","citationCount":"0","resultStr":"{\"title\":\"Quantitation of Cannabidiol (CBD) in brain regions and plasma following intranasal administration of a CBD nanoformulation.\",\"authors\":\"Gunjan Upadhyay, Oksana Fihurka, Pranav Patel, Juan Sanchez-Ramos\",\"doi\":\"10.1186/s42238-025-00308-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background and objective: </strong>Delivering therapeutic drugs to the brain for neurological disorders remains challenging due to the restrictive nature of the blood-brain barrier (BBB). Intranasal (IN) nanoparticle delivery may enhance the bioavailability of lipophilic cannabidiol (CBD), addressing limitations associated with systemic administration.</p><p><strong>Methods: </strong>Further optimization of nanoparticle properties is necessary to enhance brain uptake and therapeutic potential for neurological disorders. Following IN administration of the nanoformulation, C57BL/6 male mice (3-6 months old, n = 4/group) were euthanized at 2, 4, and 8 h. Plasma, olfactory bulb (OB), hippocampus (HP), striatum (STR), and cortex (CTX) were collected and analyzed for CBD and 7-COOH-CBD using liquid chromatography-mass spectrometry (LC-MS). Two-way analysis of variance with Tukey's multiple comparisons was used for statistical analysis.</p><p><strong>Results: </strong>CBD levels in the brain peaked at 4 h (5788 ng/mg), while 7-COOH-CBD reached its highest concentration at 2 h (3080 ng/mg). In plasma, maximum CBD levels were detected at 4 h (797 µg/mL), whereas 7-COOH-CBD peaked at 2 h (893 µg/mL). Despite measurable brain penetration, only 0.12% of the administered dose reached brain tissue, with 15.94% retained in plasma.</p><p><strong>Conclusion: </strong>This is the first study to provide the quantification of CBD and its 7CBD-COOH in various brain regions following IN administration of a CBD nanoformulation. While the approach facilitated brain delivery, overall bioavailability remained low. The use of four mice per group is a limitation that may impact the internal validity of these findings. This study aimed to develop a novel hydrophilic CBD nanoformulation for IN delivery and quantify its distribution and its major metabolite, 7-carboxy-cannabidiol (7CBD-COOH) in distinct brain regions and in plasma of mice.This methodology has the potential to overcome the limits of conventional CBD administration, providing a more effective treatment strategy for targeting brain diseases.</p>\",\"PeriodicalId\":101310,\"journal\":{\"name\":\"Journal of cannabis research\",\"volume\":\"7 1\",\"pages\":\"63\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2025-08-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12372218/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of cannabis research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1186/s42238-025-00308-5\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of cannabis research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s42238-025-00308-5","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

摘要

背景与目的:由于血脑屏障(BBB)的限制性,将治疗性药物输送到脑部治疗神经系统疾病仍然具有挑战性。鼻内(IN)纳米颗粒递送可能提高亲脂性大麻二酚(CBD)的生物利用度,解决与全身给药相关的局限性。方法:进一步优化纳米颗粒的性质是必要的,以提高大脑的吸收和治疗神经系统疾病的潜力。给药后,于2、4和8小时对C57BL/6雄性小鼠(3-6月龄,n = 4/组)实施安乐死。收集血浆、嗅球(OB)、海马(HP)、纹状体(STR)和皮质(CTX),采用液相色谱-质谱(LC-MS)分析CBD和7-COOH-CBD的含量。采用Tukey多重比较的双向方差分析进行统计分析。结果:脑内CBD浓度在4 h达到峰值(5788 ng/mg), 7-COOH-CBD浓度在2 h达到最高(3080 ng/mg)。在血浆中,4 h时检测到最大CBD水平(797µg/mL),而7-COOH-CBD在2 h时达到峰值(893µg/mL)。尽管可以测量到脑渗透,但只有0.12%的给药剂量到达脑组织,15.94%留在血浆中。结论:本研究首次提供了在给药CBD纳米制剂后不同脑区CBD及其7CBD-COOH的定量研究。虽然这种方法促进了脑输送,但总体生物利用度仍然很低。每组使用4只小鼠是一个限制,可能会影响这些发现的内部有效性。本研究旨在开发一种新的亲水CBD纳米制剂,并定量其在小鼠不同脑区和血浆中的分布及其主要代谢物7-羧基大麻二酚(7CBD-COOH)。这种方法有可能克服传统CBD给药的局限性,为针对脑部疾病提供更有效的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Quantitation of Cannabidiol (CBD) in brain regions and plasma following intranasal administration of a CBD nanoformulation.

Quantitation of Cannabidiol (CBD) in brain regions and plasma following intranasal administration of a CBD nanoformulation.

Quantitation of Cannabidiol (CBD) in brain regions and plasma following intranasal administration of a CBD nanoformulation.

Quantitation of Cannabidiol (CBD) in brain regions and plasma following intranasal administration of a CBD nanoformulation.

Background and objective: Delivering therapeutic drugs to the brain for neurological disorders remains challenging due to the restrictive nature of the blood-brain barrier (BBB). Intranasal (IN) nanoparticle delivery may enhance the bioavailability of lipophilic cannabidiol (CBD), addressing limitations associated with systemic administration.

Methods: Further optimization of nanoparticle properties is necessary to enhance brain uptake and therapeutic potential for neurological disorders. Following IN administration of the nanoformulation, C57BL/6 male mice (3-6 months old, n = 4/group) were euthanized at 2, 4, and 8 h. Plasma, olfactory bulb (OB), hippocampus (HP), striatum (STR), and cortex (CTX) were collected and analyzed for CBD and 7-COOH-CBD using liquid chromatography-mass spectrometry (LC-MS). Two-way analysis of variance with Tukey's multiple comparisons was used for statistical analysis.

Results: CBD levels in the brain peaked at 4 h (5788 ng/mg), while 7-COOH-CBD reached its highest concentration at 2 h (3080 ng/mg). In plasma, maximum CBD levels were detected at 4 h (797 µg/mL), whereas 7-COOH-CBD peaked at 2 h (893 µg/mL). Despite measurable brain penetration, only 0.12% of the administered dose reached brain tissue, with 15.94% retained in plasma.

Conclusion: This is the first study to provide the quantification of CBD and its 7CBD-COOH in various brain regions following IN administration of a CBD nanoformulation. While the approach facilitated brain delivery, overall bioavailability remained low. The use of four mice per group is a limitation that may impact the internal validity of these findings. This study aimed to develop a novel hydrophilic CBD nanoformulation for IN delivery and quantify its distribution and its major metabolite, 7-carboxy-cannabidiol (7CBD-COOH) in distinct brain regions and in plasma of mice.This methodology has the potential to overcome the limits of conventional CBD administration, providing a more effective treatment strategy for targeting brain diseases.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
6.20
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信