Pharmaceutical companies assign a budget for activities and promotions that aim to change the prescription habits of the physicians to choose the most suitable medications for their patients, which will eventually grow their sales.

The study's objectives were to explore physicians' and medical representatives' perspectives on the criteria of impactful professional PP and the factors influencing the interaction between physicians and medical representatives.

Qualitative in-depth interviews with flexible probing techniques were carried out in 2023. A semi-structured, open-ended interview questionnaire was used to interview physicians and medical representatives (MRs) from different private clinics in several

The plant known as Portulaca grandiflora L belongs to the family of flowering plants known as (Portulacaceae). It is a resilient plant that grows well in harsh environments and serves as a traditional remedy in various nations. Eleven O'clock, Moss-rose, Sunplant, gaddi roja, and Neelakeera are just a few of the popular names that are used to refer to this plant across the globe. The primary concern of the present investigation was establishing the presence of lupeol as a new metabolite in the Iraqi Portulaca grandiflora plant, which is triterpenes, have shown significant efficacy as anti-inflammatory, anti-cancer, anti-microbial, cholesterol-lowering, wound healing, and antidiabetic agents. One hundred grams of the ent

      Recently, targeted medication delivery applications have effectively used self-assembled nanoparticles (NPs). In this study, poloxamer 407 and silk sericin protein were mixed in various proportions in the presence of dimethyl sulfoxide (DMSO) to create nine formulas of self-assembled nanostructures that could transport the hydrophobic anticancer medication paclitaxel (PTX). The produced NPs were then examined to determine their size distribution, percent of entrapment efficiency (EE%), morphology, compatibility and in vitro drug release studies. The selected formula was spherical and had a particle size (145 nm), a PDI of (0.25). and EE% of 82. The FT-IR data show that PTX and excipients are compatible, and the in

The synergistic effect of the bergenin compound, derived from the Crassula ovata plant, and the docetaxel drug in vitro cell line was assessed in this study. The bergenin compound was extracted using a Soxhlet device and 85% ethanol, then was identified and isolated using a high-performance liquid chromatograph. Docetaxel is regarded as a potent chemotherapy treatment that was licensed in 1996 to treat a variety of cancers, including prostate cancer, by preventing microtubular depolymerization and reducing the impact of bcl-2 and bcl-xL gene expression. It is considered one of the most effective chemotherapy treatment for prostatic cancer. However, it has adverse effects, including febrile neutropenia or myelosuppressio

Targeting histone deacetylase enzymes (HDACs) is an effective way to treat a variety of diseases, including cancer. A number of HDAC inhibitors (HDACi) have been clinically used. Most of the clinically used HDACi are pan-inhibitors and have poor pharmacokinetic properties. Therefore, several attempts are ongoing to develop new HDACis with optimum structural features to overcome the structural limitations. In this work, six new triazole-based compounds (k1-k6) were proposed via special modification of common pharmacophores of HDACi using 1,2,4-triazole as a zinc-binding group (ZBG), diverse group in CAP group, and hydrophobic linker. These compounds were analyzed by docking study

Artificial intelligence (AI) offers significant benefits to biomedical research and academic writing. Nevertheless, using AI-powered writing aid tools has prompted worries about excessive dependence on these tools and their possible influence on writing proficiency. The current study aimed to explore the academic staff’s perspectives on the impact of AI on academic writing.

This qualitative study incorporated in-person interviews with academic faculty members. The interviews were conducted in a semi-structured manner, using a predetermined interview guide consisting of open-ended questions. The interviews were done in person with the participants from May to November 2023. The data was analyzed using thematic analysis.

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                 Lercanidipine HCl, a third-generation calcium channel blocker, blocks calcium entry into smooth muscle L-type calcium channels. This action leads to a decrease in blood pressure and induces peripheral vasodilation. Lercanidipine HCl belongs to the Biopharmaceutical classification system class II category of drugs. It is practically insoluble in water and has high solubility in methanol. The oral bioavailability of lercanidipine HCl is 10%, and irregular absorption due to its poor solubility and significant first-pass metabolism. This study aimed to produce and evaluate the nanosuspension of lercanidipine HCl with improved solubility and dissolution rates. The research used the solvent/antisolvent precipit

Self-nanomicellizing solid dispersion is a new formulation that combines the advantages of solid dispersion and nanomicelles strategies to increase drug oral bioavailability. The strategy involves utilizing a suitable carrier to create a solid dispersion that self-assembles into nanomicelles when it comes into contact with gastrointestinal fluids. Rebaudioside A is a steviol glycoside that has been reported to possess nano carrier-like characteristics by being self-assembled into nanomicelles in aqueous solutions. Canagliflozin is a novel sodium-glucose cotransporter-2 inhibitor approved for treating patients with type 2 diabetes. Its oral administration is associated with variable and poor absorption, owing primarily to insolubility in

Acemetacin (ACM) is classified as a non-steroidal anti-inflammatory drug (NSAID). It is an indomethacin glycolic ester that is transformed into indomethacin in vivo. The analgesic, antipyretic, and anti-inflammatory properties of the ACM are attributed to its prostaglandin inhibitory action. Acemetacin belongs to biopharmaceutical classification system (BCS) class II drugs, which are characterized by having high permeability but poor aqueous solubility. The purpose of this study was to develop acemetacin nanoparticles (ACM NPs) for enhanced solubility and rate of dissolution. The solvent-anti-solvent approach was used to formulate the nanoparticles. Two stabilizers were used to prepare ACM NPs (sodium deoxycholate (SDC) and Solu

     A new series of 2-(2-fluoro-[1,1'-biphenyl]-4-yl)propanoic acid derivatives were synthesized to enhance their Anti-Microbial activities. The new flurbiprofen hydrazon compounds (4a-e) prepared by reacting flurbiprofen ethyl ester with hydrazine hydrate to yield flurbiprofen hydrazid(3). Then compound (3) reacted with several aromatic aldehydes in absolute ethanol in presence of a small amount of glacial acetic acid to yield final compounds (4a-e). Each final compound was examined for its Anti-Microbial efficiency against G(+)ve bacteria (Streptococcus pyogenes, Staphylococcus aureus), G(-)ve bacteria (Escherichia coli, Klebsiella

The goal of the extant revision was to explore the influence of  caffeic acid (CA) extracted from Arctium lappa L. on lipid profile and histology of aorta  in rats .  Analytical study demonstrated a high percentage of both chlorogenic and caffeic acid in the 80 % methanol extract of the aerial parts (leaves and stems) of Arctium lappa L. from the family Asteraceace.  Hypolipidemic activity of caffeic acid was studied against cholesterol induced hypercholesterolemia in Wistar albino rats for thirty days. Rats were separated into normal group (A), hypercholesterolemic positive controller group (B). While, the rest three groups (C, D and E) attended as hypercholesterol

The Chemistry of heterocyclic sulphur and nitrogen containing compounds have a great role in the  field of scientific studies, The 2-amino 5-mercapto-1,3,4-thiadiazole ring for instance, has gained more importance in recent years because  they are considered as potent biologically active nucleus. In this study disulfide derivative can be obtained by oxidation with hydrogen peroxide of thiol group of the heterocyclic 2-amino 5-mercapto-1,3,4-thiadiazole ring to obtain compound (3) with expected antibacterial  activity. In order to use it as a diazo component to prepare some new bis azo compounds as possible antibacterial  agents, the reaction of two primary amino groups on both sides of disulfide dimer with sodium nitr

Diabetes mellitus is a global problem nowadays due to increase the disease cases all over the world, in both the developed and developing countries which may affect the quality of life (QOL ) of diabetic patients. This study was conducted to assess the quality of life of patients with type 2 diabetes mellitus (DM) and to determine some selected clinical and sociodemographic factors that affect the quality of life of these patients in Al Hila city-Iraq. This was a cross sectional study in which 100 patients with type 2 diabetes mellitus attending diabetic outpatient clinics of Merjan Teaching Hospital-Al Hila. To assess the quality of life of those diabetic patients, the World Health Organizations Quality of Life Assessment (WHOQOL) was a

The development of new cephalosporins with improved activity against resistant microbes, such as, MRSA (methicillin resistant Staph. aureus), P. aeruginosa, is of high potential. Chemical synthesis of two new series of thiadiazole linked to cysteine (series 1) and cephalosporins containing thiadiazole linked to cysteine through disulfide bond (series 2) were achieved. The chemical structures of the synthesized compounds were confirmed using spectral (FT-IR, ¹H-NMR) and elemental microanalysis. The incorporation of privileged chemical moieties, such as, thiadiazole, Schiff base, cysteine and sulfonamide, has been found to have great contribution to the antimicrobial activities. Compounds of series 1 (1

β-Adrenergic blocking agents, mostly comprising of β-amino alcohols, are of pharmaceutical significance and have received major attention due to their utility in the management of cardiovascular disorders including hypertension, angina pectoris, cardiac arrhythmias and other disorders related to the sympathetic nervous system. Most compounds available for clinical use belong to the aryloxypropanolamine series, which is considered the second generation of β-blocking agents. The present study includes the synthesis of compounds with an N-substituted oxypropanolamine moiety attached to the 1, 3, 4-thiadiazole derivatives. According to this information, eight compounds were synthesized and characterized by IR spectra and elemental m

A rapid, sensitive and without extraction spectrophotometric method for determination of clonazepam (CLO) in pure and pharmaceutical dosage forms has been described. The proposed method was simply depended on charge transfer reaction between reduced CLO (n-donor) and metol (N-methyl-p-aminophenol sulfate) as a chromogenic reagent (π- acceptor). The reduced drug, with zinc and concentrated hydrochloric acid, produced a purple colored soluble charge-transfer complex with metol in the presence of sodium metaperiodate in neutral medium, which has been measured at λmax 532 nm. All the variables which affected the developed and the stability of the colored product such as concentration of reagent and oxidant, temperature and time of rea

A series of new coumarin and N-amino-2-quinolone derivatives have been synthesized. The reaction of coumarin (1) with excess of  Hydrazine hydrate 98% yielded 1-amino-2-quinolone (2), Compound (2) was reacted with different Sulfonyl chloride to yield Sulfonamides [ N-(2-oxoquinolin-1(2H)-yl) methane sulfonamide (3), N-(2-oxoquinolin-1(2H)-yl) Benzene sulfonamide (4) and 4-methyl-N-(2-oxoquinolin-1(2H)-yl) benzene sulfonamide (5) ], while  reaction of  2-(4-methyl-2-oxo-2H-chromen-7-yloxy) acetic acid (8) with different amines yielded compounds [  2-(4-methyl-2-oxo-2H-chromen-7-yloxy)-N-(2-oxoquinolin-1(2H)-yl) acetamide (9) and N-(5-methyl-1,3,4-thiadiazol-2-yl)-2-(4-methyl-2-oxo-2H-chromen-7-yloxy)acetamide (10) ] th

The flaxseed oil contains alpha-linolenic acid, lignans and flavonoids. It possesses anti-inflammatory, antioxidant, and tumor-suppressive effects. The purpose of this research was to explore the anti-proliferative effect of flaxseed oil alone and flaxseed oil in combination with mefenamic acid on human umbilical vein endothelial cells and Kaposi sarcoma cells and to identify the vascular endothelial growth factor gene expression. The anti-proliferative effects of flaxseed oil alone and in combination with mefenamic acid were investigated in vitro by the 3-(4, 5-Dimethyl thiazol-2-yl)-2, 5-diphenyl tetrazolium bromide assay. The effects of flaxseed oil alone and its combinatio

         This study aims to encapsulate atenolol within floating alginate-ethylcellulose beads as an oral controlled-release delivery system using aqueous colloidal polymer dispersion (ACPD) method.To optimize drug entrapment efficiency and dissolution behavior of the prepared beads, different parameters of drug: polymer ratio, polymer mixture ratio, and gelling agent concentration were involved.The prepared beads were investigated with respect to their buoyancy, encapsulation efficiency, and dissolution behavior in the media: 0.1 N HCl (pH 1.2), acetate buffer (pH 4.6) and phosphate buffer (pH 6.8). The release kinetics and mechanism of the drug from the prepared beads was investigated.All prepare

Alteration in the backbone structure of the endogenously released opioid peptides Leu⁵/Met⁵ enkephalins may result in compounds having comparable profile of pharmacological activity but with different physicochemical properties and side effects. Phthalyl amino acid and phthalyl esters are among the derivatives that have been synthesized and evaluated for their antibacterial and antifungal activities.This study was conducted to evaluate the possible analgesic activity of phthalyl-tyrosyl-glycin sodium that has been recently synthesized by our team.The study was carried out on 24 albino mice using hot plate method. The animals were allocated in to three groups; the first group received saline and represent a control g

Combination therapy with a dipeptidyl peptidase–4 inhibitor and metformin or metformin+ glibenclamide results in substantial and additive glucose- lowering effects in Iraqis patients with type 2 diabetes mellitus . This study evaluated the glycemic control by using two groups of  combinations of drugs metformin + glibenclamide and metformin + sitagliptin in Baghdad teaching hospital / medical city. 68 T2DM patients and 34 normal healthy individuals as control group were enrolled in this study and categorized in to two treatment groups. The group 1 (34 patients ) received ( metformin 500 mg three times daily + glibenclamide 5 mg twice daily ) and the group 2 (34 patients) received (metformin 500 mg three times daily + sitaglip

The term of heterocyclic chemistry focuses only on heterocyclic compounds, which consider as a percentage of organic chemistry, they equal to greater than sixty-five. These compounds are widely founded in nature and most of them are important to life. In the past few years, scientist fused on 1,2,4-triazoles and their condensed heterocyclic ring due to their medicinal significance, 1,2,4-triazole containing Sulphur atom is one of the important heterocyclic moieties due to its broad range of biological activities also their derivatives can accommodate one of the alternatives as electronic effect as exchanges of the electronic density (electron donating or withdrawing) groups ; for all what mentioned above they are consider as a core molec

Herbal medicine, a complementary and alternative medicine component (CAM), has become popular worldwide, and the population has dramatically increased its utilization. Its widespread use within the general community makes it crucial to recognize how pharmacists can satisfy customers' information needs and lead to the quality use of complementary medicines within the pharmacy setting. Thus, this study was planned to evaluate knowledge, practice, and attitude toward herbal products among community pharmacists practicing in Bagdad and several other Governments in Iraq to evaluate the current pharmacist's role in patient counseling on the one hand; and predicting factors preventing pharmacists from occupying their full scope of practice on t

Silymarin (SM), a natural polyphenolic flavonoid, shows antidiabetic and lipid-lowering characteristics with poor aqueous solubility and bioavailability. In the current investigation, SM-incorporated ethosomes (ETO) were designed and optimized using design expert version 8.0.7.1 to overcome these pitfalls. The SM-ETO were synthesized and subjected to determine the physical appearance, percent drug entrapment, size distribution, negative charge potential, morphology study, powder crystallinity and phase transition behaviour. Following optimization, SM-ETO were added to the carbapol-containing gel and examined for pH, rheology study, drug content and in-vitro drug release study. The results manifested that SM-ETO batches did not s

Spanlastic is a modern drug delivery that combines vesicular and nanoparticulate characteristics with numerous advantages over topical applied conventional vesicular systems in terms of stablility, penetration flexibility, and targeting. Meloxicam (MX) is a potent non-steroid anti-inflammatory drug that is frequently utilized for the short- and long-term treatment of chronic pain and inflammatory diseases including rheumatoid arthritis. However, the oral administration of MX often includes several adverse effects, including gastrointestinal disturbances and ulceration. Thus, the aim is a preparation of proper formula for MX-loaded spanlastics via studying the formulation variables that may affect their properties using the ethanol inject

Indonesia is known as one of the countries which has the biggest biodiversity worldwide. The aim of this study is to determine the characteristics and the strength of carrageenan as a tablet binder from Kappaphycus alvarezii seaweed that is produced by farmers in the South Lampung District, Province of Lampung. Carrageenan that was produced was characterized by its physical, chemical, and functional characteristics. Carrageenan then was formulated in a tablet dosage form as a binder and compared to tablets that used carbopol as a binder. The data obtained from the physical, chemical, and functional characteristics was described qualitatively and the test results of some parameters from the physical characteristic tablets were an

Mucopolysaccharidosis (MPS) is a rare heterogenous progressive genetic disorder, which is a subset of lysosomal storage diseases with a consequence of glycosaminoglycans building-up inside the lysosomes which attributed to enzymes absence or deficiency.  This study was aimed to identify mutations that associated with mucopolysaccharidosis of Iraqi children in different Iraqi metabolic centers. While in concerning to the genetic study, the eligible patients who had no genetic analysis and who are not received hematopoietic stem cells transportation were enrolled in this study for molecular confirmation of mucopolysaccharidosis disorders and reporting the existence of any new variants among Iraqi patients. Consequentl

 Abstract

Hydrogels, being a drug delivery system , have great significance, particularly for the topical application in the treatment of open wounds. Their non-adhesiveness, moisture retention, and exudate absorption properties make them ideal for wound healing applications. Using a novel synthesis method, the biomedical hydrogels carrageenan/alginate (κC-Sa) and carrageenan/alginate/ZnO (κC-Sa/ZnO) were synthesized through modified free radical polymerization with acrylic acid as a cross-linker. The hydrogels were characterized using FTIR, FE-SEM, EDX, TEM, and photographic images. κC-Sa and κC-Sa/ZnO were applied as wound healers for injured rats. The synthesized hydrogels have a microstru

Abstract:

Background: Drug toxicity and chemotherapeutic side effects negatively impact the quality of life of breast cancer patients.

Objectives: to evaluate the efficacy of pharmaceutical Interventions (PI) on quality of life (QOL)Among chemotherapy intake breast cancer women.

 Method: A pre-post interventional study was carried out at the chemotherapy ward of Alhabobi Hospital in Alnasiriyah City. Eligible patients received comprehensive pharmaceutical care and a self-compiled Breast Cancer Patients Medication Knowledge Guide pamphlet. Each pat

         The antidiabetic thiozolidinediones (TZDs) a class of peroxisome proliferators-activated receptor (PPAR) ligands has recently been the focus of much interest for their possible role in regulation of inflammatory response. The present study was designed to evaluate the anti-inflammatory activity of pioglitazone in experimental models of inflammation in rats. The present study was conducted to evaluate the anti inflammatory effect of TZDs (pioglitazone 3mg/Kg) on acute, sub acute and chronic model of inflammation by using egg-albumin and formalin–induced paw edema in 72 rats, relative to reference drugs Dexamethasone 5mg/Kg and Piroxicam 5mg/Kg. In each inflammation model, 24 rats wer