Science

DRUG DELIVERY TO RESPIRATORY SYSTEM PDF DOWNLOAD

Author: Kagajind Samujinn
Country: Myanmar
Language: English (Spanish)
Genre: Career
Published (Last): 26 December 2006
Pages: 185
PDF File Size: 10.43 Mb
ePub File Size: 12.12 Mb
ISBN: 589-8-30987-950-5
Downloads: 9524
Price: Free* [*Free Regsitration Required]
Uploader: Vigar

See our Privacy Policy and User Agreement for details.

The open end of the test tube was closed with the nasal membrane of the pig by tying it with a thread. Small, unchanged drugs easily pass through this layer but large, charged drugs are difficult to cross it.

Nasal Drops Nasal drops are one of the most simple and convenient systems developed for nasal delivery. The absorption of peptides like angiotensin II, bradykinin, caulein, arnosine, enkephalin, vasopressin and calcitonin are improved by pr e-pared into enamine derivatives, these agents showed absorption enhancement with prod rug approach.

Microparticles spread on the tissue specimen and the prepared glass slide was hung on drug delivery to respiratory system pdf download of the groves of a USP tablet disintegration test apparatus. Published on Oct 4, Local application of drug is another advantage of this system. Enzymatic degradation in nasal cavity. Visibility Others can see my Clipboard. Now customize the name of a clipboard to store your clips. Does increasing the lipophilicity of peptides enhance their nasal absorption.

The prod rug undergoes enzymatic transformation to release the active medicament, when it crosses the enzymatic and membrane barrier. The absorption enhancers like salts and fusidic acid derivatives also shows enzyme inhibition activity to increase the absorption and bioavailability of the drug.

Overall, this can result in increased absorption efficacy and stability and reduced toxicity of the active ingredient.

Pulmonary Drug Delivery | Respiratory Tract | Lung

B The interior of a well in a blisterdisk. Slideshare uses cookies to improve functionality and performance, and to provide you with relevant advertising.

The AERx dosage form.

Microspheres are mainly increase the absorption sysetm bioavailability by adhering to the nasal mucosa and increase the nasal residence time of drug. Rfspiratory has been reported that nasal drops deposit human serum albumin in the nostrils more efficiently than nasal drug delivery to respiratory system pdf download. Metered—dose Inhaler MDI 3. Cationic liposome’s are having good permeation capacity than negatively charged anionic liposome’s. The stabilizers such as sucrose are also added in the formulation to prevent denaturation during prolonged storage.

The effect should be temporary and reversible. The chemical modification of drug molecule has been commonly used to modify the physicochemical properties of a drug such as molecular size, molecular weight, Pka and solubility are favourable to improve the nasal absorption of drug. In the treatment of obstructive respiratory diseases, pulmonary delivery can minimize systemic side effects, provide rapid response and minimize the required dose respiatory the drug delivery to respiratory system pdf download is delivered directly to the conducting zone of the lungs.

Pulmonary Drug Delivery

No notes for slide. The main disadvantage of this system is the lack of the dose precision and therefore nasal drops may not be suitable for prescription products.

The microspheres prepared by using polymers like delivefy, chitosan, biodegradable starch microspheres successfully improved the bioavailability of various drugs.

Because of advancement in applications of pulmonary drug delivery it is useful for multiple diseases. The particles size and morphology for suspensions of the drug and viscosity of the formulation determine the choice of pump and drug delivery to respiratory system pdf download assembly. Drug delivery to respiratory system.

Show related SlideShares at end. To modify drug structure to change physicochemical properties. So pulmonary drug delivery is best route of administration. The core technology was initially developed to overcome the patient pd required for metered-dose inhalers and the inspiratory effort required for first-generation dry powder inhalers in treating asthma.