Abstract

Emerging infectious diseases have become a major global problem with public health and economic consequences. It is an urgent need to develop new anti-infective therapies. The natural diterpene carnosol exhibit a wide variety of interesting antibacterial and antiviral properties, and it is considered a theoretical inhibitor of COVID-19 Mpro. However, this compound is present in the family Lamiaceae in low quantities. To obtain carnosol in concentrations high enough to develop pharmacological studies, we evaluated the efficiency of a micropropagation protocol of Rosmarinus officinalis using a solid medium and a temporary immersion system (TIS), as well as the effect of 6-benzylaminopurine (6-BAP) and α-naphthaleneacetic acid (NAA) on the growth of shoots. Moreover, we developed and validated an analytical method to quantify carnosol using the H-point standard additions method in the high-performance liquid chromatography diode array detector (HPLC-DAD). After 30 days of culture, TIS produced the maximum number of shoots per explant (24.33 ± 1.15) on a liquid medium supplemented with 6-BAP at 5.0 mg L−1. Next, we also evaluated the effect of immersion time and frequency for TIS. After 72 days of culture, the best results were obtained with an immersion cycle of 1 min every 12 h, yielding 170.33 ± 29.40 shoots. The quantification of carnosol on the samples was performed at a flow rate of 1.2 mL min−1 using binary isocratic mobile phase system 60:40 (v/v) 10 mM formic acid (pH 3.0) (A) and acetonitrile (B) on a reverse-phase column. The content of carnosol in the in vitro cultures was around 8-fold higher than in the wild plant. The present study represents an efficient alternative method to obtain carnosol for its pre-clinical and clinical development.

Highlights

  • According to the World Health Organization (WHO), the infectious diseases cause more than 5 million deaths globally every year

  • The results showed significant differences between both culture systems when they were supplemented with the same plant growth regulators (PGR)

  • temporary immersion system (TIS) culture system regenerated the maximum number of shoots on a liquid medium supplemented with 6-BAP at 5.0 mg L−1 (24.33 ± 1.15 shoots per explant; Table 1, entry 6)

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Summary

Introduction

According to the World Health Organization (WHO), the infectious diseases cause more than 5 million deaths globally every year. The presence of both carnosic acid and carnosol is essential for the antibacterial activity of R. officinalis, [7]. All the available information suggest that these abietane diterpenes are very promising antiviral and antimicrobial agents to treat present or future infectious diseases such as COVID-19, the main problem for the clinical applications of these compounds it is that they are very expensive compounds obtained from natural sources. To solve this problem, we think that the in vitro culture of R. officinalis cells is an alternative to obtain these secondary metabolites in abundance and high purity. We develop a very fast and high-resolution separation system by high-performance liquid chromatography, connected to a diode array detector (HPLC-DAD) using reverse phase, and a sensitive and selective analytical method to quantify carnosol by using H-point standard additions method in HPLC-DAD

Evaluation of the Different Culture Systems
Evaluation of Different Immersion Frequencies
Quantification of Carnosol in Callus Extracts Obtained by Maceration
Result
General Experimental Procedures
Material and Culture
Experimental Design
Statistical Analysis
Extraction of Carnosol and TLC Analysis
Instrumentation and HPLC Conditions
Preparation of Standards and Samples
Validation of HPLC Method
Quantification of Carnosol
Conclusions
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