Poster presentation
149
STUDIES OF TANNIES IN THE LIQUID EXTRACT
“EXTRADENT”
Sh.S. Yuldasheva, N.A. Yunuskhodjayeva, N.E. Yunuskhodjiyeva,
D.R. Gulyamova
Tashkent Pharmaceutical Institute, st. Aybek 45, Tashkent, Uzbekistan
Ensuring the proper quality of medicinal products largely
depends on the proper
organization of control, its effectiveness and efficiency,
as well as on the level of
requirements laid down in the regulatory documentation (RD) and the methods of
analysis used. We have developed an anti-inflammatory, hemostatic liquid extract from
herbs Knotweed (
Polygonum hydropiper
L.)
,
shepherd's purse (
Bursa pastoris
)
,
marigold flowers (
Calendula officinalis
L
.
) and nettle leaves (
Urtica dioica
L.). These
plants contain various biologically active substances. The purpose of our study was to
study the content of tannins in the liquid extract "Extradent".
According to literary sources, we know that when determining tannins, the titrometry
method is most widely used. We have developed an HPLC method for the identification
and quantification of tannins using gallic acid.
Gallic acid was determined using a SHIMADZU LC-2030
Plus high-performance
liquid chromatograph. Separation is carried out on a 150
4.6 mm HPLC ACE 3 C18
column with a particle size of 3 µm. Mobile phase water: acetonitrile at a ratio of 80:20,
detection wavelength 272 nm, analysis time 30 minutes, pH of the mobile phase - 2.7,
flow rate of the mobile phase - 1.0 ml/min, volume of injected sample - 10 ml.
Preparation of a standard solution: 5 mg of gallic acid (t.n.) are placed in a
volumetric flask with a capacity of 5 ml and dissolved in a mixture of water: methanol
in a ratio (9:1) adjusted to the mark to obtain a standard solution of 1 mg/ml. 2 ml of the
resulting solution is placed in a volumetric flask with a capacity of 20 ml, diluted to the
mark with solvent and filtered.
Preparation of the test solution: 1 ml of the liquid extract is placed in a volumetric
flask with a capacity of 25 ml, dissolved with a mixture of water: methanol (9:1),
adjusted to the mark with a solvent. 5 ml of the resulting solution is placed in a flask
with a capacity of 20 ml and adjusted to the mark with the solvent and filtered. The
retention time of 2.1 min of gallic acid in the liquid extract
is comparable to the
retention time of a standard sample. The content of gallic acid in the composition of the
liquid extract is calculated by the following formula:
Conclusions: developed a method for the qualitative and quantitative determination
of gallic acid in the liquid extract "Extradent" by HPLC. It was revealed that the content
of gallic acid was 0,2% . The relative error was 1,68 %.
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