Farmacología de productos naturales: un enfoque reciente en Calotropis gigantea y Calotropis procera

The authors are thankful to the Dr. Ritu Gilhotra, Principal, School of Pharmacy, Suresh Gyanvihar University, Jaipur, Rajasthan, India. For valuable guidanceIntroduction: Since ancient times, people have used medicinal plants to treat varied diseases. Medicinal plants are the important source of drugs, and many of them that are currently available in the pharmaceutical market are obtained from plant sources. Calotropis gigantea and Calotropis procera are small shrub, which are used conventionally to treat many diseases such as cancer, diabetes and intestinal disease in African and Asian countries. There have been always an increased focus on primary health care: basic health care which is effective and affordable by developing countries. Objective: This paper aims to review the pharmacological and pharmacognostical features of Calotropis gigantea and Calotropis procera Method: Brief review on recent literature carried out using Scopus, Google scholar. Result and Discussion: Several studies provide evidence of their antioxidant, analgesic, anti-inflammatory, anti-diarrheal, anticonvulsant, anti-malarial, hepatoprotective, antitumor, antimicrobial and antinociceptive properties. Conclusion: Species of Calotropis not widely recognized showed different pharmacological actions, due to the presence of effective secondary metabolites.Introducción: Desde la antigüedad, las personas han utilizado plantas medicinales para tratar diversas enfermedades. Las plantas medicinales son la fuente importante de los fármacos, y muchas de ellas, que están actualmente disponibles en el mercado farmacéutico, se obtienen de fuentes vegetales. Calotropis gigantea y Calotropis procera son arbustos pequeños que se utilizan convencionalmente para tratar muchas enfermedades como el cáncer, la diabetes y las enfermedades intestinales en países africanos y asiáticos. Siempre se ha prestado una mayor atención a la Atención Primaria de salud: la atención básica de la salud es eficaz y asequible para los países en desarrollo. Objetivos: Este trabajo tiene como objetivo revisar las características farmacológicas y farmacognosóticas de Calotropis gigantea y Calotropis procera. Método: Breve revisión de la literatura reciente realizada utilizando Scopus, Google scholar. Resultado y discusión: Varios estudios proporcionan evidencia de sus propiedades antioxidantes, analgésicas, antiinflamatorias, antidiarreicas, anticonvulsivas, antipalúdicas, hepatoprotectoras, antitumorales, antimicrobianas y anti-nociceptivas. Conclusión: Especies de Calotropis no ampliamente reconocido mostraron diferentes acciones farmacológicas, debido a la presencia de metabolitos secundarios efectivos

A RAPID, SENSITIVE AND VALIDATED ULTRA PERFORMANCE LIQUID CHROMATOGRAPHY AND TANDEM MASS SPECTROMETRY METHOD FOR DETERMINATION OF PAROMOMYCIN IN MICE PLASMA: APPLICATION TO PHARMACOKINETIC STUDY

Objective: To develop and validate simple, sensitive, accurate and selective UPLC-MS/MS method for quantification of paromomycin (PARO) in mice plasma.Methods: Precipitation method was used for the extraction of plasma samples, an aliquot of 25 µl plasma samples was extracted using 10% perchloric acid in water. Chromatographic separation was performed using waters acquity ultra-performance liquid chromatography (UPLC) columns, BEH HILIC (50 mm× 2.1 mm, 1.7 µm) by a gradient mixture of acetonitrile and water (both containing 0.005% v/v trifluro acetic acid) as a mobile phase at the flow rate of 0.2 ml/min. The analyte was protonated in the positive electrospray ionization (ESI) interface and detected in multiple reactions monitoring (MRM) modes using the transition m/z 308.60-455.30.Results: The method had a short chromatographic run time of 3 min. Calibration curves were linear over wide ranges of 50.51-5019.22 ng/ml. The between and within-batch precision and accuracy of the method was determined by using 4 quality control samples, the highest % CV observed was 11.06. The mean recovery values are 78.17, 101.17 and 92.58 at low, medium and high-quality control levels; respectively.Conclusion: It was concluded that the developed and validated UPLC-MS/MS method was rapid, sensitive, accurate, precise, linear, and specific. Therefore, this method can be used for quantification of PARO in mice plasma with various advantages over the reported methods

Evaluation of Polyherbal Anticancer Tablets: A Review

Cancer is a malignant abnormal growth of cells, one of the most dreaded and complex diseases. It concerns with several tempo spatial changes in cell composition, which finally lead to neoplasia. Various types of cancers have been reported. Chemotherapy, radiation, and/or surgery may cure them. Herbal remedies are supposed to be harmless as they cause fewer complications and are less likely to habitual. Antioxidant compositions of therapeutic plants show the anticancer activity and therefore, use of different proportions of the active components to formulate various standardized preparation with single or multiple components for their synergistic effects play a crucial role in curing cancer. Evaluation parameters to assess the in vitro anticancer activity includes Caspase-3, Caspase-9, alamar blue, LDH assay, XTT assay, sulforhodamine-B assay, MTT assay, DNA fragmentation assay, neutral red uptake cytotoxic assay, tryphan blue assay. Evaluation of dried extract or granules includes bulk density, tapped density, Carr’s index, Hausner’s ratio, angle of repose while the tablets evaluated by drug-excipient compatibility study by FT-IR, stability studies, hardness, thickness, weight variation, friability, disintegration time and dissolution test

LIQUID CHROMATOGRAPHY TANDEM-MASS SPECTROMETRY METHOD DEVELOPMENT AND VALIDATION FOR SIMULTANEOUS ANALYSIS OF PARACETAMOL, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, CHLORPHENIRAMINE MALEATE, AND AMBROXOL HYDROCHLORIDE IN BULK AND IN TABLET DOSAGE FORM

Objective: The objective is to study liquid chromatography tandem-mass spectrometry (LC/MS/MS) method for simultaneous quantification of paracetamol (PCM), guaifenesin (GUA), phenylephrine hydrochloride (PE), chlorpheniramine maleate (CPM), and ambroxol hydrochloride (AMB) in tablet dosage form developed and validated as per the International Conference on Harmonization Q2 (R1) guideline. Methods: The chromatograms were developed using a gradient mobile phase of WATER:methanol. Flow rate used was to 0.3 ml/min. Quantitation was performed using multiple reaction monitoring (MRM) mode to study parent to product ion transition, for paracetamol. (m/z 152.0 ≥ 110.0), guaifenesin (m/z 199.0 ≥163.0), phenylephrine hydrochloride (m/z 168.0≥ 150.0), chlorpheniramine maleate (m/z 275.0 ≥ 230.0) and ambroxol hydrochloride (m/z 379.0 ≥ 263.8). Results: The retention times were found to be 1.76, 1.81, 1.90, 2.10, and 2.33 min for PCM, GUA, PE, CPM, and AMB, respectively. The linearity of the method was found to be in the concentration range of 10–200 ng/ml for PCM, GUA, PE, CPM, and AMB. Percentage relative standard deviation values for repeatability and intermediate precision studies were below 2%. Conclusion: Developed method was found to be robust, precise, accurate, rapid and can be used to analyze fixed-dose tablet formulation used in the study.Â

Gastroretentive drug delivery systems a potential approach for antihypertensive drugs: An updated review

Oral drug delivery system (DDS) is the preferred route of administration of drugs, but poor bioavailability (BA) of orally administered drugs is still a challenging one, though extensive advancements in drug discovery process are made. Drugs with narrow absorption window in the gastrointestinal tract have poor absorption. Gastric emptying of dosage forms is an extremely variable process and ability to prolong and control the emptying time is a valuable asset for dosage forms, which reside in the stomach for a longer period of time than conventional dosage forms. Therefore, gastroretentive DDSs (GRDDSs) have been developed, which prolong the gastric emptying time. Most of the antihypertensive drugs have short half-life, short gastric residence time, low BA, and narrow absorption window. GRDDS can be a viable option for management of hypertension for several antihypertensive drugs. Several techniques such as floating DDS, low-density systems, raft systems, mucoadhesive systems, high-density systems, super porous hydrogels, and magnetic systems have been employed. These forms are expected to remain buoyant on gastric content without affecting the intrinsic rate of emptying. This results in prolonged gastric retention time of floating forms which improve BA of drug and also improve clinical situations. Prolonged gastric retention not only improves the BA and reduces drug waste but also improves solubility for drugs that are less soluble in a high pH environment. It has applications also for local drug delivery to the stomach and proximal small intestines. Gastroretention helps to provide better availability of new products with new therapeutic possibilities and substantial benefits for patients. Hence, it can be concluded that GRDDS promises to be a potential approach for antihypertensive drugs. This review mainly focuses on the different types of GRDDS used for management of hypertension and also includes the updated compiled study of different antihypertensive drugs explored as GR dosage forms