Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 May 20;22(1):143.
doi: 10.1186/s12906-022-03619-9.

Anti-inflammatory and anti-nociceptive effects of Cinnamon and Clove essential oils nanogels: an in vivo study

Affiliations

Anti-inflammatory and anti-nociceptive effects of Cinnamon and Clove essential oils nanogels: an in vivo study

Fariba Esmaeili et al. BMC Complement Med Ther. .

Abstract

Background: Cinnamon (Cinnamomum zeylanicum) and Clove (Syzygium aromaticum) essential oils are two medicinally important plant-derived substances with a wide range of biological properties. Besides, nanoemulsion-based gels have been widely used to increase topical drug delivery and effectiveness.

Methods: This study aimed to explore the anti-inflammatory effect (paw edema test) and the anti-nociceptive effect (hot plate and formalin test) of nanoemulsion-based gels containing the essential oils in the animal model. Cinnamon and Clove essential oils nanoemulsions with droplet sizes of 28 ± 6 nm and 12 ± 3 nm were first prepared. By adding carboxymethylcellulose (3.5% w/v), the nanoemulsions were then gelified. Finally, the nanogels were characterized by ATR-FTIR analysis and were used as topical pre-treatment before induction of inflammation or pain in acute and chronic analgesic experimental studies.

Results: The paw edema and formalin findings showed that the nanogels formulations possess significant anti-nociceptive and anti-inflammatory effects.

Conclusion: The prepared nanogels could be considered as analgesic drugs for inhibiting the inflammation and pain of diseases.

Keywords: Analgesics; Nanomedicine; Painkiller; Paw edema test.

PubMed Disclaimer

Conflict of interest statement

All authors declare no conflict of interest.

Figures

Fig. 1
Fig. 1
Left curve: Cinnamon EO nanoemulsion with mean droplet size ± SD: 28 ± 6 nm; Right curve: Clove EO nanoemulsion with droplet size ± SD: 12 ± 3 nm
Fig. 2
Fig. 2
ATR-FTIR spectra of the samples (CMC: carboxymethylcellulose, NG: nanogel)
Fig. 3
Fig. 3
The acute anti-nociceptive activity of cinnamon-NG and clove-NG on reaction latency in hot plate test; no significant differences between samples. Investigated groups (n = 6) include distilled water (D.W.: control group), blank gel, cinnamon-NG, and clove-NG. The data were presented as mean ± SE
Fig. 4
Fig. 4
Comparison of acute and chronic phases results of formalin test after treatment with distilled water (D.W.: control group), cinnamon-NG, and clove-NG. Each value represents mean ± SEM, *P < 0.05, **P < 0.01, ***P < 0.001
Fig. 5
Fig. 5
The effect of cinnamon-NG and clove-NG on rat nociceptive behavior. Groups (n = 6) include distilled water (D.W.: control group), cinnamon-NG, and clove-NG. Each value represents mean ± SE
Fig. 6
Fig. 6
Comparison of licking time in acute and chronic phases of the formalin test after treatment with distilled water (D.W.: control group), blank gel, clove-NG, and cinnamon-NG. Each value represents mean ± SEM, *P < 0.05, **P < 0.01
Fig. 7
Fig. 7
The effect of cinnamon-NG and clove-NG in a rat paw edema induced by carrageenan model. Rats (n = 6) were pre-treated with distilled water (D.W.: control group), blank gel, cinnamon-NG, and clove-NG. The measurements were obtained at 1, 2, 3, 4, and 5 hours after the carrageenan sub-plantar injection (1%, 100 μl). *P < 0.05

Similar articles

Cited by

References

    1. Chen L, Deng H, Cui H, Fang J, Zuo Z, Deng J, Li Y, Wang X, Zhao L. Inflammatory responses and inflammation-associated diseases in organs. Oncotarget. 2018;9(6):7204. doi: 10.18632/oncotarget.23208. - DOI - PMC - PubMed
    1. Zhong J, Shi G. Regulation of inflammation in chronic disease. Front Immunol. 2019;10:737. doi: 10.3389/fimmu.2019.00737. - DOI - PMC - PubMed
    1. Jancalek R. Signaling mechanisms in mirror image pain pathogenesis. Ann Neurosci. 2011;18(3):123–127. doi: 10.5214/ans.0972.7531.11183010. - DOI - PMC - PubMed
    1. Shin J, Cho H, Hwang SW, Jung J, Shin CY, Lee S-Y, Kim SH, Lee MG, Choi YH, Kim J. Bradykinin-12-lipoxygenase-VR1 signaling pathway for inflammatory hyperalgesia. Proc Natl Acad Sci U S A. 2002;99(15):10150–10155. doi: 10.1073/pnas.152002699. - DOI - PMC - PubMed
    1. Oliveira CC. Understanding pain and human suffering. Rev Bioét. 2016;24:225–234. doi: 10.1590/1983-80422016242122. - DOI

LinkOut - more resources