SOLID LIPID NANOPARTICLES (SLNs): SLN’S are recent advances to vesicular drug delivery systems. It consist of solid lipid core surrounded by a phospholipid layer. The lipid used should be biocompatible and exist in solid state at room temperature and body temperature. Slns are not easily phagocytised by reticulo endothelial system and hence remain in the systemic circulation for longer time period. Slns can be linked to specific ligands which will recognise receptors present on specific cells and hence achieve targeted drug delivery thus enhancing bioavailability of the drug. Sln can be used to incorporate both hydrophilic as well as hydrophobic drugs. COMPONENTS: 1.Lipids: Triacyl glycerols: Tricaprin, Trilaurin Acyl glycerols: Glycerol monostearate, Glycerol behenate, Glycerol palmitostearate. Waxes: Cetyl palmitate. Hard fats: Witepsol H, Witepsol W. 2. Surfactants: Soya lecithin, egg lecithin, …show more content…
Thus this formulation improved oral bioavailability by directly entering systemic circulation thereby reducing hepatic metabolism. Anil .B. Jindal et al prepared asymmetric lipomer using Gantrez AN 119 as the polymer and glyceryl monostearate as the lipid composition21. Due to its size and lipid composition lipomer can enter into the lymphatic circulation and treat many splenic diseases as well as cancers and enhance the delivery of si- rna molecules which otherwise becomes difficult to target at the site of action. LIPOSOMES: Liposomes are most widely used colloidal vesicular systems having many applications in the field of medicine. Liposomes can deliver the drug through oral, ocular, parentral and topical route. Liposomes consist of a phospholipid bilayer surrounding the aqueous core. It can load hydrophilic as well as lipophilic drug due to its amphiphilic
It is soluble in water and N,N-dimethyl formamide; slightly soluble in methanol; very slightly soluble in ethanol, acetone, and acetonitrile; and insoluble in isopropanol and isopropyl
The difference in this chemical and physical properties will aid in their separation. Processes like solubility, gravitational filtration and recrystallization will be used to separate the substances present in Panacetin. The melting and boiling point of the substances will help in concluding on which of these compounds will be presented at the end of experiment. Procedure and observation The Panacetin content was weighed approximately 3.0493g and transferred to the Erlenmeyer flask; 75ml of dichloromethane (CH¬2CL2) was added to the content. The dichloromethane (CH2Cl2) dissolved the sucrose, leaving the active unknown agent and aspirin behind.
10 Things To Consider While Using Clenbuterol Looking for bodybuilding and have a thought of using Clenbuterol for it? Yes, Clenbuterol is a powerful supplement to use as itself but most of the people prefer using it in a stack which can enhance the overall results. Using Clenbuterol in a stack of several supplements can help you in faster muscle mass increase and also help to cut the weight easily. You can combine it with steroids or supplements such as dieta con clembuterol to achieve the desired result.
Lab Report 5: Acetylsalicylic Acid (Aspirin) Synthesis Name: Divya Mehta Student #: 139006548 Date Conducted: November 19th 2014 Date Submitted: November 26th 2014 Partner’s Name: Kirsten Matthews Lab Section: Wednesday 2:30 L9 IAs Name: Brittany Doerr Procedure: For the procedure, see lab manual (CH110 Lab Manual, Fall 2014) pages 96-98. Wilfrid Laurier University Chemistry Department. Fall 2014. Acetylsalicylic Acid (Aspirin) Synthesis.
To conclude, many of the ingredients and additives discussed in this paper are
Introduction The plasma membrane is an outer layer that is formed around the cell. It is composed of phospholipids and proteins and this is structure is crucial to all cells in our bodies. The plasma membrane acts as a border and more importantly is responsible for what is allowed to enter and leave the cell. The ability to allow specific molecules to enter and leave the cell is known as selective permeability and it is the phospholipids that make this unique ability possible.
Experiment 4: Formal Report Preparation and Recrystallisation of Aspirin Aim of the experiment: In this experiment, a pure sample of aspirin is to be obtained through esterification to synthesise the sample, then purify the sample by recrystallisation. Lastly, determine the melting point of the sample to characterise the aspirin. Introduction: Background Aspirin (acetylsalicylic acid) is an aromatic compound that contains an ester- functional group and a carboxylic acid- functional group. Aspirin is commonly used as a pain reliever (analgesic), an anti-inflammatory, an anti-coagulant (prevent platelet aggregation) and an antipyretic (to reduce fever) pill.
EXENATIDE Pharmacology Exenatide is a synthetic form of naturally occurring peptide Exendin-4 in Gila monster 16. It has 50% of sequence homology with native GLP-1 with the substitution of amino acid Arg with Gly at 2nd position, which provides resistance against DPP-4 and a half life of ~2-4hr. It is administered 60min before breakfast and dinner, with a predominant effect of reduction in PPG (Postprandial glucose) 17. Exenatide is rapidly absorbed following subcutaneous administration and eliminated through kidneys after proteolytic degradation by dipeptidyl peptidase IV.18 Clinical Pharmacology
CARBOHYDRATES Carbohydrates are the most abundant biomolecules on Earth. Each year, photosynthesis converts more than 100 billion metric tons of CO2 and H2O into cellulose and other plant products. Carbohydrates are widely distributed in plants and animals; they have important structural and metabolic roles. In plants, glucose is synthesized from carbon dioxide and water by photosynthesis and stored as starch or used to synthesize the cellulose of the plant cell walls. Animals can synthesize carbohydrates from amino acids, but most are derived ultimately from plants.
However, the narrow therapeutic window and multiorgan toxicity has limited it from further clinical use. In order to increase its therapeutic index, different kinds of triptolide-loaded delivery systems have been developed, which has been verified to change the pharmacokinetics of triptolide and decrease the toxicity. The pharmacokinetic study of a triptolide-loaded delivery system in mice showed that a targeted tissue accumulation and longer residence time were found in triptolide-loaded lipid emulsion [62]. The AUC0-t of triptolide-loaded lipid emulsion increased 2.19 folds, suggesting that the triptolide-loaded lipid emulsion does improve the biodistribution, accumulation and therapeutic efficacy in pancreas. Moreover, the levels of triptolide-loaded lipid emulsion in heart, lung and kidney were lower than that of the triptolide group, which would reduce the toxicity of triptolide in the above tissues.
Question 1 (Difference Between Means): Is there a significant difference between drug type in mean relative-change* of Cholesterol from screening to follow up? It will be important to investigate the effect of drug since the company whose data is being analyzed conducted the study to understand the effect of two comparable cholesterol lowering drugs. Other important aspect was to examine other factors like weight and BMI to understand their influence on cholesterol level.
Artificial membranes are models of lower variability. The simple structure lipid membranes or the more complex structure ones (e.g. liposomes consisting of SC lipids fixed to a supporting filter (Matsuzaki et al., 1993)) have the disadvantage of absence of pores. Another recent option is artificial membranes consisting of silicone and poly (2-hydroxyethyl methacrylate) which allow drug penetration through the lipid and the pore route (Hatanaka et al., 1990; Hatanaka et al.,
The primary surface-active material found in surfactant is the phospholipid, dipalmitoylphosphatidylcholine
Den active substance is insoluble in vatten. Coenzym often used in the form of oil solutions, which are much easier to melt than tabletizirovannye or powder form of the coenzyme, which must be taken with fatty
This nature of membranes is mainly because of the membrane structure. It is the phospholipids and the molecules present in the membrane that bring about fluidity of membranes. Fluidity mainly depends on temperature, nature of fatty acids and length of the fatty acid chain.