US2007190158A1PendingUtilityA1

Pharmaceutical compositions in particulate form

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Assignee: BECTON DICKINSON COPriority: Nov 19, 2001Filed: Mar 26, 2007Published: Aug 16, 2007
Est. expiryNov 19, 2021(expired)· nominal 20-yr term from priority
A61K 9/0078A61K 47/26A61K 9/1652A61K 9/0075A61K 9/0043A61K 9/1688A61P 31/16A61P 31/12A61K 9/1694A61K 9/1623A61K 9/0019A61K 9/19A61K 9/14
61
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Claims

Abstract

A method of preparing a pharmaceutical composition is described, comprising 1) atomizing a liquid formulation of a therapeutic agent to produce an atomized formulation; 2) freezing said atomized formulation to form solid particles; and 3) drying said solid particles at about atmospheric pressure to produce a powder, wherein said drying is performed in the presence of vibration, internals, mechanical stirring, or a combination thereof. Another method is described, comprising 1) atomizing a liquid formulation of a therapeutic agent to produce an atomized formulation; 2) freezing said atomized formulation to form solid particles; and 3) drying said solid particles to produce a powder; wherein the atomized formulation comprises droplets having an average mean diameter of between about 35μ and about 300μ, and/or the powder comprises dried particles having an average mean diameter of between about 35μ and about 300μ. Compositions made by the above methods, and methods of using the compositions, are also described.

Claims

exact text as granted — not AI-modified
1 . A method of preparing a pharmaceutical composition in the form of a powder within a chamber, the method comprising the steps of: 
 a) atomizing a liquid formulation of a therapeutic or prophylactic agent to produce atomized droplets;    b) freezing the atomized droplets by introducing a cold medium into the chamber to form frozen particles; and    c) collecting and drying the frozen particles to produce a dry powder.    
   
   
       2 . The method of  claim 1 , wherein the liquid formulation comprises more than one therapeutic or prophylactic agent.  
   
   
       3 . The method of  claim 1 , wherein the cold medium is a gas.  
   
   
       4 . The method of  claim 1 , wherein the therapeutic or prophylactic agent is suspended or dissolved in the liquid formulation.  
   
   
       5 . The method of  claim 1 , wherein the frozen particles are collected on a filter.  
   
   
       6 . The method of  claim 5 , wherein the frozen particles are partially dried after being collected on the filter.  
   
   
       7 . A method of creating a powder within a chamber, the method comprising the steps of: 
 providing a flow of liquid droplets containing a powder forming ingredient to form a flow of liquid droplets;    treating the liquid droplets with a flow of coolant inside the chamber to freeze the liquid droplets to form frozen particles prior to deposition;    depositing the frozen particles on a collector; and    after deposition of the frozen particles, drying the deposited frozen particles to form a dry powder.    
   
   
       8 . The method of  claim 7  in which the flow of liquid droplets contains more than one powder forming ingredient.  
   
   
       9 . The method of  claim 7  in which the coolant is a gas.  
   
   
       10 . The method of  claim 7  in which the powder forming ingredient is suspended or dissolved in the carrier liquid.  
   
   
       11 . The method of  claim 7  in which the frozen particles are collected on a filter.  
   
   
       12 . The method of  claim 11  in which the frozen particles are substantially dried after being collected on the filter.

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