pharmaceutical excipient

Sodium dodecyl sulfate(Sodium lauryl sulfate) is a pharmaceutical excipient that is biologically inactive and improves the stability, solubility and processability of pharmaceutical preparations.

Citric Acid Monohydrate is a tricarboxylic acid found in citrus fruits. Citric acid is used as an excipient in pharmaceutical preparations due to its antioxidant properties. It maintains stability of active ingredients and is used as a preservative.

Sorbitan monooleate is a pharmaceutical excipient, a lipophilic nonionic surfactant, and is often used as an emulsifier in cosmetics, food and pharmaceuticals.

Poly(acrylic acid) serves as an effective corrosion inhibitor for pure cast aluminium in acidic environments through its adsorption onto the metal's surface. Additionally, this compound functions as an excipient within the pharmaceutical industry, utilized in roles such as a coating material and release blocker. Pharmaceutical excipients, also known as pharmaceutical auxiliaries, are chemical substances employed in drug formulation alongside the active pharmaceutical ingredients to enhance the stability, solubility, and manufacturability of the products. These excipients also influence the absorption, distribution, metabolism, and elimination (ADME) processes of drugs [1] [2].

Cellulose can be used as an excipient. Pharmaceutical excipients, or pharmaceutical auxiliaries, refer to other chemical substances used in the pharmaceutical process other than pharmaceutical ingredients. Pharmaceutical excipients generally refer to inactive ingredients in pharmaceutical preparations, which can improve the stability, solubility and processability of pharmaceutical preparations. Pharmaceutical excipients also affect the absorption, distribution, metabolism, and elimination (ADME) processes of co-administered drugs [1] .

Polyoxyethylene Sorbitan Monostearate, an ester derived from the saturated fatty acid stearic acid (C18:0), serves multiple roles in pharmaceutical formulations, including as a surfactant, emulsifier, solubilizer, and wetting agent. As a pharmaceutical excipient—an inert substance that enhances the stability, solubility, and processability of drug formulations—it plays a crucial role in affecting the absorption, distribution, metabolism, and elimination (ADME) processes of drugs [1] [2].

Maltodextrin (dextrose equivalent 16.5-19.5) serves as an excipient in pharmaceutical applications. Excipients, also known as pharmaceutical auxiliaries, are chemical substances utilized in drug formulation alongside active pharmaceutical ingredients. They primarily enhance the stability, solubility, and processability of drug preparations, while also influencing the absorption, distribution, metabolism, and elimination (ADME) of co-administered drugs [1].

Trisodium phosphate dodecahydrate serves as a corrosion inhibitor for iron in 0.1 M NaClO4 solutions, effective under both aerated and deaerated conditions. Additionally, it acts as an excipient in pharmaceutical formulations, functioning primarily as a pH regulator and buffer. These excipients, also known as pharmaceutical auxiliaries, are substances utilized in the pharmaceutical manufacturing process besides the active pharmaceutical ingredients. They are crucial for enhancing the stability, solubility, and processability of pharmaceutical products. Moreover, pharmaceutical excipients play a significant role in influencing the absorption, distribution, metabolism, and elimination (ADME) of co-administered drugs, thereby affecting their efficacy and safety [1] [2].

DSPE-Fluor 488 is a phospholipid known for its excellent biocompatibility and distinctive amphiphilic properties, making it an ideal form and excipient in pharmaceutical formulations for enhanced therapeutic outcomes. It is utilized in the study of drug delivery.

DSPE-Amide-PEG-Rhodamine (MW 2000) is a phospholipid known for its excellent biocompatibility and pronounced amphiphilicity, making it a key and suitable form or excipient in pharmaceutical formulations to achieve enhanced therapeutic outcomes. DSPE-Amide-PEG-Rhodamine (MW 2000) can be employed in drug delivery research.

DOPE-PEG-Rhodamine B (MW 5000) is a phospholipid known for its excellent biocompatibility and pronounced amphiphilic properties, making it an ideal and primary excipient in pharmaceutical formulations for enhanced therapeutic outcomes. It is applicable in the research of drug delivery systems.

Ethyl cellulose (viscosity 10 cP) is a non-toxic and biodegradable polymer known for its unique capabilities in forming oil gels, delivering active ingredients, and film-forming in the food and pharmaceutical industries. It can serve as a pharmaceutical excipient, such as a coating agent, flavoring agent, and tablet filler.

Ethyl cellulose (viscosity 300 cP) is a non-toxic, biodegradable polymer notable for its unique properties of oil gelation, active ingredient delivery, and film formation in the food and pharmaceutical industries. It serves as a pharmaceutical excipient and can be used as a coating agent, flavoring, and tablet filler.

DOPE-PEG-COOH (MW 1000) is a phospholipid characterized by excellent biocompatibility and notable amphiphilic properties, making it an ideal and pivotal excipient or dosage form in pharmaceutical formulations for enhanced therapeutic outcomes. It is applicable in studies related to drug delivery.

DOPE-mPEG (MW 1000) is a phospholipid known for its excellent biocompatibility and significant amphiphilic properties, making it a suitable and primary excipient in pharmaceutical formulations to enhance therapeutic outcomes. It can be utilized in research focused on drug delivery.

DOPE-PEG-Amine (MW 3400) is a phospholipid known for its excellent biocompatibility and distinct amphipathic properties. These characteristics make it an ideal and primary excipient or dosage form in pharmaceutical formulations, enabling enhanced therapeutic outcomes. Additionally, DOPE-PEG-Amine (MW 3400) can be utilized in drug delivery research.

DOPE-PEG-Mal (MW 1000) is a phospholipid characterized by excellent biocompatibility and notable amphiphilic properties, making it an ideal primary dosage form or excipient in pharmaceutical formulations for enhanced therapeutic outcomes. It is employed in studies related to drug delivery.

Maltodextrin, dextrose equivalent 16.5-19.5 (Standard) is the standard substance of Maltodextrin, dextrose equivalent 16.5-19.5, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Maltodextrin (dextrose equivalent 16.5-19.5) serves as an excipient in pharmaceutical applications. Excipients, also known as pharmaceutical auxiliaries, are chemical substances utilized in drug formulation alongside active pharmaceutical ingredients. They primarily enhance the stability, solubility, and processability of drug preparations, while also influencing the absorption, distribution, metabolism, and elimination (ADME) of co-administered drugs .

D-Glucamine, 98% (1-Amino-1-deoxy-D-glucitol, 98%) is an amino sugar derivative used as an excipient in pharmaceutical preparations. Additionally, it serves as a substrate for studies investigating the sugar transporter protein pathways.

1,4-Anhydro-D-xylitol is a sugar alcohol compound derived from xylitol, a natural sweetener found in various fruits and vegetables. In the food and pharmaceutical industries, it is commonly utilized as a low-calorie sweetener and excipient, serving as a filler or binder in drug formulations. Additionally, its potential applications in the development of biodegradable plastics and other sustainable materials have been explored.