Licorice Compound Traditional Syrup: Formulation and Development of Analysis Method

Background and objective: Glycyrrhiza glabra L. (licorice) is one of the most important medicinal plants for respiratory disorders. It is used alone or in combination with other species. In the present investigation, an herbal syrup containing licorice, fennel, and fig was formulated according to Ir...

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Main Authors: Behnaz Keramatian (Author), Leila Ara (Author), Homa Hajimehdipoor* (Author)
Format: Book
Published: Iranian Society of Pharmacognosy, 2022-01-01T00:00:00Z.
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001 doaj_aa854cc8622f47e7ad5cf84c6ec71f8d
042 |a dc 
100 1 0 |a Behnaz Keramatian  |e author 
700 1 0 |a Leila Ara  |e author 
700 1 0 |a Homa Hajimehdipoor*  |e author 
245 0 0 |a Licorice Compound Traditional Syrup: Formulation and Development of Analysis Method 
260 |b Iranian Society of Pharmacognosy,   |c 2022-01-01T00:00:00Z. 
500 |a 2345-4458 
500 |a 2345-5977 
500 |a 10.22127/rjp.2021.294636.1739 
520 |a Background and objective: Glycyrrhiza glabra L. (licorice) is one of the most important medicinal plants for respiratory disorders. It is used alone or in combination with other species. In the present investigation, an herbal syrup containing licorice, fennel, and fig was formulated according to Iranian traditional medicine prescriptions and glycyrrhizic acid content of the syrup was quantified using a validated HPLC method. Method: Traditional syrup was prepared by decocting the mixture of licorice: fennel: fig (20, 8, 62.5 g in 100 mL). It was filtered and concentrated. Sugar was used in the syrup (40%). Quality control tests were performed and glycyrrhizic acid content of the syrup was determined using an HPLC method. The method was verified according to verification parameters, as well. Accelerated stability tests were carried out during 6 months in 40 °C. Results: The prepared syrup was brown colored with fennel odor and sweet taste. The pH, viscosity, dry residue and density were 5.13, 134.8 cP, 51.43%, 1.10 g/cm3, respectively. Glycyrrhizic acid content was 1.99 mg/mL. The HPLC method was valid according to specificity, linearity (9.3-27.9 µg/mL, r2: 0.9972), intra-day precision (RSD≤1.71%), inter-day precision (RSD: 3.31%), instrument precision (RSD: 0.82%), recovery (95.6%), LOD (1.48 µg/mL) and LOQ (4.49 µg/mL). Conclusion: The prepared syrup with suitable physicochemical and microbial characteristics is a proper candidate for producing at industrial scale after further invivo and clinical studies. Moreover, the HPLC method can be used as a validated method for quality control of the syrup. 
546 |a EN 
690 |a glycyrrhiza glabra 
690 |a hplc 
690 |a quality control 
690 |a respiratory disorders 
690 |a syrup 
690 |a validation study 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Research Journal of Pharmacognosy, Vol 9, Iss 1, Pp 111-117 (2022) 
787 0 |n http://www.rjpharmacognosy.ir/article_141594_2751a29b263758ee1e6ad5f9cae687cd.pdf 
787 0 |n https://doaj.org/toc/2345-4458 
787 0 |n https://doaj.org/toc/2345-5977 
856 4 1 |u https://doaj.org/article/aa854cc8622f47e7ad5cf84c6ec71f8d  |z Connect to this object online.