Unlock instant, AI-driven research and patent intelligence for your innovation.

Apparatus for transdermal delivery of parathyroid hormone agents

A kind of drug and transdermal technology, which is applied in the direction of drug equipment, medical science, surgery, etc., and can solve the problems of poor compliance, discomfort, and difficulties of patients

Inactive Publication Date: 2009-12-09
ALZA CORP
View PDF41 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0021] Despite the effectiveness of PTH in the treatment of diseases such as osteoporosis, there are some disadvantages and disadvantages of the prior art disclosed methods of PTH release, especially by subcutaneous injection
The main disadvantage of subcutaneous injection is the difficult and uncomfortable procedure, which often results in poor patient compliance

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Apparatus for transdermal delivery of parathyroid hormone agents
  • Apparatus for transdermal delivery of parathyroid hormone agents
  • Apparatus for transdermal delivery of parathyroid hormone agents

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0205] Release of hPTH(1-34) from coated microprojection arrays was evaluated using the hairless guinea pig (HGP) model. Microprojection arrays were fabricated using photo / chemical etching and patterning. The microprojection array used in this study has an area of ​​2 cm 2 , 320 microprojections / cm 2 , the jet body length is 200 μm. The microprojection array was divided into 25% aqueous solution of hPTH(1-34) every 2cm 2 Arrays were 40 ± 10 μg coated, with solid coating limited to the first 100 μm of the microprojections. Each coated microprojection array was mounted with a flexible polymeric adhesive backing. The resulting patch was placed on a ring positioner and onto a reusable impact applicator when applied to the HGP.

[0206] Each anesthetized HGP received the patch, which was applied to a clean skin area for 1 hour. At various time intervals after patch application, blood samples were taken. hPTH(1-34) plasma levels were determined by enzyme immunoassay (Peninsul...

Embodiment 2

[0214] Example 2 demonstrates that hPTH(1-34) drugs increase viscosity using weak acids. The interaction of the weak acid anion with the positively charged hPTH(1-34) drug leads to the formation of secondary bonds, such as hydrogen bonds, which lead to an increase in solution viscosity. The greater the number of acidic groups, the greater the number of second bonds formed between the anion and the hPTH(1-34) drug, and thus the greater the increase in viscosity. Therefore, when comparing monobasic acids, dibasic acids, tribasic acids, and tetrabasic acids, the theoretical viscosity increasing ability increases.

[0215] In this test, hPTH(1-34) preparations were spiked with various weak acid buffers. A control formulation including PTH(1-34) acetate and sucrose was also prepared. This test investigated the physicochemical properties provided by various mixtures of hPTH(1-34) with mono-, di-, and tri-acids, and the stability of solution formulations at 2-8°C for 48 hours. The...

Embodiment 3

[0221] Example 3 demonstrates that hPTH(1-34) drugs use counter ion mixtures to enhance the in vivo dissolution of hPTH-based drugs.

[0222] In solid coatings on microprojection arrays, the drug is generally present in an amount of less than about 1 mg per unit dose. After adding excipients and counter ions, the total mass of the solid coating can be less than 3 mg per unit dose.

[0223] The array is typically present on an adhesive backing that is adhered to a disposable polymeric ring retainer. The combination is typically individually packaged in a sachet or polymer casing. In addition to the combination, the package contains an atmosphere (usually inert) providing a volume of at least 3 ml. This large volume (compared to the coating volume) acts as an absorber for any volatile components. For example, at 20°C, the amount of acetic acid present in 3ml of atmosphere due to its vapor pressure is about 0.15mg. If acetic acid is used as the counterion, this amount will ge...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

Apparatus and method for the transdermal release of biologically active agents, comprising a release system having a microprojection element (30) (or system) comprising a plurality of microinjection elements (or systems) adapted to penetrate the stratum corneum into the sub-epidermal layer or the epidermis and dermis A layer of microprojections (32) (or an array thereof). In one embodiment, a PTH based drug is included in the biocompatible coating (35) applied to the microprojection member.

Description

[0001] Cross References to Related Applications [0002] This application claims U.S. Provisional Application No. 60 / 571,304 filed May 13, 2004; U.S. Provisional Application No. 60 / 585,276 filed July 1, 2004; U.S. Provisional Application No. 12, 2005 .60 / 643,660 in equity. field of invention [0003] The present invention generally relates to transdermal drug delivery systems and methods. More particularly, the present invention relates to devices and methods for the transdermal delivery of parathyroid hormone drugs. Background of the invention [0004] The active agent (or drug) is most commonly administered orally or by injection. Unfortunately, many active agents are completely ineffective or have greatly reduced efficacy when taken orally because they are not absorbed or are adversely affected before entering the bloodstream and thus do not possess the desired activity. On the other hand, direct intravenous or subcutaneous injection of drugs, while ensuring that the d...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): A61B17/20A61M37/00
Inventor M·阿梅里M·J·N·科尔米尔Y·-F·马M·坎贝里P·达多纳
Owner ALZA CORP