Effervescent Tablets Formulation of Jicama (Pachyrhizus erosus) Extract with Various Concentrations of Binders and Sweeteners

نویسندگان

چکیده

Osteoporosis is a major public health problem. Exogenous estrogen or Hormone Replacement Therapy (HRT) the potential therapy for osteoporosis. Still, patient rarely chooses this treatment because of risk breast and endometrial cancer. Phytoestrogens estrogen-like compounds, particularly isoflavones, are potentially safe alternative to HRT. Jicama (Pachyrhizus erosus) plant that contains many phytoestrogens. This research aimed determine physicochemical characteristics jicama extract in effervescent tablets with various concentrations binder sweetener. The manufacturing used raw materials extracted from 96% p.a. ethanol by maceration. then formulated (PVP 40 gelatin) sweeteners (lactose Mannitol) using wet granulation method. Based on test results properties tablets, all formula meets requirement good tablet, preferred Formula 4 0.75% PVP40 47,75% Mannitol. Ethanol can be into has developed as osteoporosis.
 Keywords: Xicama Extract, Fitoestrogen, Estrogen-like therapy, Osteoporosis, Effervescent tablet

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Hypoglycemic Effect of Jicama (Pachyrhizus erosus) Extract on Streptozotocin-Induced Diabetic Mice

The purpose of this research was to investigate the inhibitory effect of jicama extract on α-glucosidase activity, α-amylase activity, and postprandial hyperglycemia in streptozotocin (STZ)-induced diabetic mice. Jicama extract showed prominent inhibitory effects against α-glucosidase and α-amylase. The IC50 values of jicama extract against α-glucosidase and α-amylase were 0.083±0.004 and 0.091...

متن کامل

Induction of chilling injury in jicama (Pachyrhizus erosus) roots: changes in texture, color and phenolics

Storage of jicama roots at 10 °C resulted in characteristic chill-induced changes in pulp color (decreased L* values and increased chroma) and texture (increased distance to rupture) after 7–14 days. Discoloration or browning of the pulp occurred first in exterior pulp tissue and then progressed to the interior tissue. Changes in texture during storage were similar in exterior and interior pulp...

متن کامل

Formulation and evaluation of effervescent floating tablets of tizanidine hydrochloride.

Tizanidine hydrochloride is an orally administered prokinetic agent that facilitates or restores motility through-out the length of the gastrointestinal tract. The objective of the present investigation was to develop effervescent floating matrix tablets of tizanidine hydrochloride for prolongation of gastric residence time in order to overcome its low bioavailability (34-40 %) and short biolog...

متن کامل

Formulation, characterization and physicochemical evaluation of ranitidine effervescent tablets.

PURPOSE The aim of this study was to design, formulate and physicochemically evaluate effervescent ranitidine hydrochloride (HCl) tablets since they are easily administered while the elderly and children sometimes have difficulties in swallowing oral dosage forms. METHODS Effervescent ranitidine HCl tablets were prepared in a dosage of 300 mg by fusion and direct compression methods. The powd...

متن کامل

Formulation, characterization and physicochemical evaluation of potassium citrate effervescent tablets.

PURPOSE The aim of this study was to design and formulation of potassium citrate effervescent tablet for reduction of calcium oxalate and urate kidney stones in patients suffering from kidney stones. METHODS In this study, 13 formulations were prepared from potassium citrate and effervescent base in different concentration. The flowability of powders and granules was studied. Then effervescen...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: KnE medicine

سال: 2023

ISSN: ['2519-125X']

DOI: https://doi.org/10.18502/kme.v3i3.13491