WO1995016438A1 - Biphasic capsule formulation - Google Patents

Biphasic capsule formulation Download PDF

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Publication number
WO1995016438A1
WO1995016438A1 PCT/GB1994/002703 GB9402703W WO9516438A1 WO 1995016438 A1 WO1995016438 A1 WO 1995016438A1 GB 9402703 W GB9402703 W GB 9402703W WO 9516438 A1 WO9516438 A1 WO 9516438A1
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WO
WIPO (PCT)
Prior art keywords
formulation
barrier
gelucire
fill
compositions
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/GB1994/002703
Other languages
French (fr)
Inventor
Stephen George Barnwell
Simon Higginbottom
Ian Peter Whelan
Stephen John Burns
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Cortecs Ltd
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Cortecs Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to JP7516594A priority Critical patent/JPH09506606A/en
Priority to DE69429928T priority patent/DE69429928T2/en
Priority to US08/666,563 priority patent/US6153218A/en
Priority to AT95902878T priority patent/ATE213406T1/en
Priority to NZ277074A priority patent/NZ277074A/en
Priority to BR9408294A priority patent/BR9408294A/en
Priority to AU11967/95A priority patent/AU702464B2/en
Priority to EP95902878A priority patent/EP0734253B1/en
Application filed by Cortecs Ltd filed Critical Cortecs Ltd
Priority to DK95902878T priority patent/DK0734253T3/en
Priority to CA002179041A priority patent/CA2179041C/en
Publication of WO1995016438A1 publication Critical patent/WO1995016438A1/en
Anticipated expiration legal-status Critical
Priority to US10/652,834 priority patent/US20050191347A1/en
Priority to US11/734,183 priority patent/US20070202161A1/en
Ceased legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/4833—Encapsulating processes; Filling of capsules
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/4808—Preparations in capsules, e.g. of gelatin, of chocolate characterised by the form of the capsule or the structure of the filling; Capsules containing small tablets; Capsules with outer layer for immediate drug release
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/4841—Filling excipients; Inactive ingredients
    • A61K9/4858—Organic compounds

Definitions

  • the present invention relates to improved capsule formulations, in particular biphasic capsule formulations.
  • WO-A-9206680 discloses biphasic release formulations for lipophilic drugs comprising a C 12 -C 24 fatty acid and a pharmaceutically active substance. A portion of the formulation is formulated for non-sustained release and is generally in liquid form and a portion is formulated for sustained release on non-parenteral administration and will generally be a solid.
  • a pnarmaceutical formulation comprising a capsule containing at least two fill compositions, cnaracterised in that the compositions are prevented from mixing with one another.
  • the capsule fill compositions may be compositions comprising C ⁇ - C ⁇ fatty acids such as those disclosed in WO-A-9206680.
  • the invention is particularly useful when one of the fill compositions is a solid and one a liquid, especially when the solid component also comprises glycerides, for example the GELUCIRETM mixture disclosed m Example 1 of WO-A-9206680.
  • the fatty acids tend to dissolve the lower molecular weight lipids of the solid composition so that they gradually mix with tne liquid composition.
  • the progressive sol c lisation of the lower molecular weignt glycerides nto tne liquid composition slows down the rapid release characteristics of the liquid phase.
  • a modified capsule would be an adaptation of the potato starch Capill ® capsules manufactured by Capsugel Limited. In th s case, the starch capsule would be manufactured with a central partition and two open ends. This would allow two separate formulation components to be filled, each end of the capsule being sealed by the usual potato starch cap. Thus the sustained release of the active material from the solid component is retarded.
  • compositions such as those disclosed in GB Application No 9417524.7 there is the possibility of unfavourable interaction of the active ingredient, particularly f t is a protein, and tne pH ⁇ od ⁇ fy ⁇ ng agent (for instance, carbonate or bicarconate .
  • the present invention is particularly useful for such formulations .
  • the simplest method cf preventing phase mixing is to formulate both of the fill compositions as solids but of course this will not be possible in ail cases. Therefore, it is often desirable to provide some sort of physical barrier within the capsule to prevent mixing of the fill compositions.
  • the barrier may not be possible to manufacture from the same material as the capsule shell . There may be a variety of reasons for this, for example the difficulties in manufacturing a two-compartment capsule and the weakness in the capsule wall which a central barrier within the capsule may introduce. In addition, for soft gelatin capsules, the capsule walls may not be strong enough to support a central barrier in the capsule.
  • hydrophobic fill compositions it may be desirable to use a hydrophilic material as a barrier between the fill compositions.
  • a hydrophobic material will be more suitable.
  • the material used as a barrier should have a melting point such that it is a solid at any likely storage temperature. Therefore, the melting point should, at the least, be higher than 25°C
  • room temperature but it is much preferred that the material should not begin to melt until it reaches about 37°C (body temperature) .
  • a barrier formed from such a material has the advantage of easy formation since the barrier material can simply be filled into the capsules in a molten state at a temperature above its melting point and then allowed to cool and form a solid barrier.
  • the barrier material will be added to the capsule after the first fill composition has been put into the capsule but before the addition of the second fill composition so as to form an effective barrier between the two compositions.
  • the capsule is required to contain more than two fill compositions then layers of the barrier material can be added to the capsule between additions of the different f ll compositions.
  • the barrier material must, of course, be physiologically compatible since it is to be included in a pharmaceutical formulation.
  • glycerides having a transition temperature (melting point) above 37°C Materials which have been found to be particularly useful as barrier materials in capsules are glycerides having a transition temperature (melting point) above 37°C.
  • ⁇ -itable glycerides include di- and tri-glycerides, such as many of the various GELUCIRE compounds, which are hy ⁇ rogenated fatty acid esters available from Gattefosse.
  • GELUCIRE is a trade mark.
  • Other trade marks cf suitable glycerides include LABRAFIL and PRECIROL.
  • G ⁇ LUCIRE compounds and other suitable compounds having transition temperatures of from 40°C to 70°C are preferred.
  • Specific examples of exemplary GELUCIRE compounds, and their equivalents include:
  • GELUCIRE 54/02 also available as PRECIROL
  • GELUCIRE 62/05 and GELUCIRE 64/02 also available as PRECIROL WL 2155.
  • G ⁇ LUCIRE name represent the liquid/solid phase transition temperature in degrees centigrade and the second two digits represent the hydrophile/lipophile balance (HLB) value.
  • Z- ⁇ LUCIRE 44/14 has a high HLB value and is therefore relatively hydrophilic. This means that it is particularly useful as a carrier m capsules containing lipopmlic fill compositions sucn as those ⁇ escrice ⁇ m WO-A-9206680 since it will ce immiscible with both of the f ll compositions.
  • the other compounds are more suitable for use in capsules with a hydrophilic fill since tney are all relatively lipopmlic .
  • a furtner use for the nydropmlic phase barrier may be to allow the formulation of a hydrophilic drug for co- admmistration with the lipophilic delivery system described m WO-A-9206680.
  • An example of this application is the formulation and delivery of a non- memcrane damaging Pile acid (a nydrophilic material) as descnced m WO-A-9325192 together with a lipophilic drug m the lipophilic delivery system described in WO-A- 9206680.
  • the advantage cf this arrangement is for the improved delivery of drugs which undergo botn high hepatic first-pass metapolism and enterohepatic recycling •. e . g .
  • tne non-membrane damaging bile acid can attenuate the toxic effects of a drug subject to high first-pass metapolism and formulated as described m WO-A-9206680.
  • a lipopmlic barrier is used to separate hydrophilic phases it may act as a reservoir for a co-administered lipophilic drug.
  • liquid fill compositions may contain gelatin softening agents such as those described in WO-A- 9102520.
  • gelatin softening agents can be found by reference to the art of manufacturing soft gelatin capsules where sucn materials are incorporated into the mix which forms the gelatin wall.
  • Particularly suitable gelatin softening agents include glycerol, propylene glycol, glycerol mono-oleate and sorbitol .
  • the capsules may be enteric coated or otherwise protected to ensure better survival of the pharmaceutically active compound through the stomach. Any convenient enteric protection metnod may be used.
  • Capsules containing the formulation may ce coated with an enteric coat such as hydroxypropyimethylcellulose phthalate or by the commercial coating process of Pharma-Vinci A/S (Denmark) .
  • the formulations of the invention may be prepared by any suitable process cut when a solid barrier material is used then the process may comprise filling the first fill composition, the carrier material and the second fill composition sequentially into a suitable capsule.
  • a process ror tne preparation of a capsule containing at least two fill compositions separated by a barrier material comprising filling a first fill composition, the carrier material and a second fill composition sequentially into a suitable capsule.
  • Preferred barrier materials are as described above.
  • the capsule may be of any suitacle material, for example hard gelatin capsules, soft gelatin capsules and starch capsules out gelatin capsules are preferred, particularly hard gelatin capsules.
  • the following example is a iphasic rapid and sustained- release propranolol formulation similar to that described m WO 92/06680. Typically these materials melt upon neatmg, thereoy allowing tne use of conventional mixing ana pumping technology for fluid filling.
  • the oleic acid, Geiucire 50/02 and Cremophor were heated to 50°C-55°C until a clear solution was obtained.
  • Propranolol base was added with stirring, while maintaining the temperature of the mix at 50°C and continued until the propranolol base was fully dissolved.
  • Aerosil was added while stirring. A total of 272 mg of the formulation was filled into size 0 hard gelatin capsules while hot and then allowed to solidify with cooling.
  • Oleic acid was heate ⁇ witn stirring at 45°C-50°C.
  • Propranolol base was added and dissolved with stirring and allowed to cool.
  • a total of 150 mg of the liquid rapid-release formulation was then filled over the phase barrier.
  • the resulting capsules contained a solid sustained-release phase, solid phase separation barrier and liquid rapid-release phase.
  • the capsules were then sealed by gelatin banding. Following gelatin banding, the capsules may be enteric-coated as described in WO 92/06680.
  • test-method For evaluating the dispersion behaviour of the experimental formulations, a test-method was devised based upon the USP XXII dissolution test for tablets and capsules. The aim of the test was to subject the samples to an environment similar to that in the intestine. Dispersion in 5 nours was selected as a satisfactory total release time for the test samples. This was based on the understanding that lympnatic absorption occurs predominantly m the small intestine.
  • the dissolution apparatus as specified by the USP XXII (apparatus 2) was used with Sorensens phosphate buffer, pH 6.8 containing 0.2% sodium cholate and 0.1% sodium deoxycholate, equilibrated to 37°C.
  • the total volume of buffer added to each dissolution vessel was 900 ml, with a paddle rotation speed of 70 rpm.
  • the paddle height was a ⁇ iusted so that tne top edge of the blade was level with tne surface of the liquid.
  • the test sample was dropped ⁇ nto Hi-issoiution medium and the rotation of the paddle started. The test sample was allowed to float freely at the liquid surface throughout the test.
  • a 5 ml aliquot of the dissolution medium was removed and replaced with 5 ml of fresh buffer solution.
  • Each 5 ml sample was initially filtered through a 1.2 ⁇ M coarse filter and subsequent 1.2 ⁇ M fine filter.
  • the absorbance of the filtered solution was then determined at 290nm using a UV at 290 nm using a UV spectrophotometer.
  • the propranolol concentration in the dissolution medium was calculated using a pre-determined calibration curve for propranolol.
  • A Example 1 with phase barrier.
  • B Example 1 without phase barrier,
  • the rapid-release phase is formulated as a solid, using Geiucire *3 ' 33/01, which melts on heating above 30°C allowing (i) capsule filling to take place using conventional mixing and pumping technology, and (ii) 1 A
  • the modified rapid-release phase was manufactured by heating cieic acid at 45-50°C with stirring. Propranolol base and Geiucire ® 33/01 were added with stirring until completely dissolved. The molten rapid-release phase was maintained above 37°C until filled into capsules already containing the solid sustained-release phase described in Example 1. A total of 300 mg of the modified sustained- release phase containing Geiucire ® 33/01 was filled into size 0 hard gelatin capsules while hot and then allowed to solidify with cooling. The capsules were then sealed by gelatin banding. Following gelatin banding, the capsules may be enteric-coated as described in WO-A- 9206680 and Burns et al , International Journal of Pharmaceutics, 110: 291-296 (1994) . EXAMPLE 4 - Dissolution Studies Using Solid Rapid-Release Phase System
  • Example 3 The same dissolution method as described in Example 2 was used to evaluate capsules containing the biphasic rapid and sustained-release preparation described in Example 3.
  • Table 3 show that at 25°C the dissolution profile cf a c pnasic formulation is maintained for at least 12 months.
  • Table 4 shows that at 30°C, close to the melting point of the modified rapid-release phase containing Geiucire ® 33/01, there is a small deterioration m initial release rate. However, the overall biphasic release characteristics of the formulation are maintained.

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Abstract

Capsule formulations are provided containing at least two different fill compositions which are prevented from mixing either by providing both of the fill compositions as solids or by providing a physical barrier which separates the fill compositions so that they are prevented from mixing. The invention has the advantage that two different formulations can be provided in a single capsule without one of the formulations having an adverse effect on the other.

Description

Biphasic capsule formulation
The present invention relates to improved capsule formulations, in particular biphasic capsule formulations.
WO-A-9206680 discloses biphasic release formulations for lipophilic drugs comprising a C12-C24 fatty acid and a pharmaceutically active substance. A portion of the formulation is formulated for non-sustained release and is generally in liquid form and a portion is formulated for sustained release on non-parenteral administration and will generally be a solid.
The formulations are extremely effective for the administration of lipophilic pharmaceutically active substances greatly enhancing oral bioavailibility of propranolol. These results have been published (Barnwell et al, J-. Controlled Release, 28, 306-309 (1994) ) , but it has been discovered that there are certain problems with the stability of the compositions even when stored at ambient temperature .
After capsules containing biphasic formulations such as those described in WO-A-9206680 have ' been stored for periods of greater than 3 months at ambient temperature, there is a decline in in vitro dissolution performance compared with initial values. The level of propranolol released from the formulation after 12 months' storage at ambient temperature was found to be reduced by 50% compared with initial values. In contrast, prolonged storage of capsules containing only the liquid rapid- release phase and capsules containing only the solid sustained release phase did not result in any change in dissolution profile This unstable release profile is therefore a prcoiem cn±y witn bipnasic formulations and represents a serious αrawaack m the development of such formulations since, clearly, a pharmaceutical formulation wnich is not stable under ambient storage conditions is of limited use m practice.
On investigation, it appeared that the deterioration in tne release profile naα arisen because, unexpectedly, the two phases of the formulation had become mixed during the storage of the capsules and the mixing of the phases had caused the release characteristics of both parts of the formulation to deteriorate. Deterioration was characterised by a visible intermixing between the two pnases and a decline m in vitro dissolution performance. The rate of intermixing between the liquid rapid and solid sustained-release phases of the formulation was accelerated at elevated storage temperatures, eg 37°C, but much reduced at 4°C.
Therefore, m a first aspect of the invention there is provided a pnarmaceutical formulation comprising a capsule containing at least two fill compositions, cnaracterised in that the compositions are prevented from mixing with one another.
The capsule fill compositions may be compositions comprising C^ - C^ fatty acids such as those disclosed in WO-A-9206680. The invention is particularly useful when one of the fill compositions is a solid and one a liquid, especially when the solid component also comprises glycerides, for example the GELUCIRE™ mixture disclosed m Example 1 of WO-A-9206680. In that case, the fatty acids tend to dissolve the lower molecular weight lipids of the solid composition so that they gradually mix with tne liquid composition. The progressive sol c lisation of the lower molecular weignt glycerides nto tne liquid composition slows down the rapid release characteristics of the liquid phase. It also leaves m the solid phase only the higher molecular weight glycende components which do not easily erode to allow the release of the remaining fatty acid and the active material . An example of a modified capsule would be an adaptation of the potato starch Capill® capsules manufactured by Capsugel Limited. In th s case, the starch capsule would be manufactured with a central partition and two open ends. This would allow two separate formulation components to be filled, each end of the capsule being sealed by the usual potato starch cap. Thus the sustained release of the active material from the solid component is retarded. These changes in drug release may be monitored using an m vitro dissolution method such as that described in Example 2 below
However, there may be other reasons for wishing to separate the two fill compositions, for example they may contain different active compounds or different excipients whicn interact in an unfavourable ranner and therefore the present invention is not limited to compositions sucn as those described in WO-A-9206680.
For example, with compositions such as those disclosed in GB Application No 9417524.7 there is the possibility of unfavourable interaction of the active ingredient, particularly f t is a protein, and tne pH ~ιodιfyιng agent (for instance, carbonate or bicarconate . Thus, the present invention is particularly useful for such formulations . The simplest method cf preventing phase mixing is to formulate both of the fill compositions as solids but of course this will not be possible in ail cases. Therefore, it is often desirable to provide some sort of physical barrier within the capsule to prevent mixing of the fill compositions.
However, there are problems with this approach. One problem is that the placing of a physical barrier between two compositions in a capsule often leads to the collapse of the capsule walls and any barrier which has this effect is of no use whatever.
Secondly, it is important to ensure that any material used as a physical barrier between fill compositions in a capsule does not interact with the fill compositions themselves. One solution which may overcome this problem is to provide a barrier of the same material as the capsule . This may be achieved by manufacturing capsules having two compartments and will be particularly effective for hard gelatin capsules and starch capsules.
In some cases, it will not be possible to manufacture the barrier from the same material as the capsule shell . There may be a variety of reasons for this, for example the difficulties in manufacturing a two-compartment capsule and the weakness in the capsule wall which a central barrier within the capsule may introduce. In addition, for soft gelatin capsules, the capsule walls may not be strong enough to support a central barrier in the capsule.
In such cases a barrier must be introduced into the capsule after manufacture and this will usually be done as the capsule is filled. This will retain the advantage cf low manufacturing cost cf the capsules whilst still separating the fill compositions and preventing them from mixing.
The choice of material for the barrier is important and several factors must be taken into account. For example, if hydrophobic fill compositions are used, it may be desirable to use a hydrophilic material as a barrier between the fill compositions. On the other hand, if the fill compositions are hydrophilic in nature, then a hydrophobic material will be more suitable.
It is also highly desirable that the material used as a barrier should have a melting point such that it is a solid at any likely storage temperature. Therefore, the melting point should, at the least, be higher than 25°C
(room temperature) but it is much preferred that the material should not begin to melt until it reaches about 37°C (body temperature) .
A barrier formed from such a material has the advantage of easy formation since the barrier material can simply be filled into the capsules in a molten state at a temperature above its melting point and then allowed to cool and form a solid barrier. The barrier material will be added to the capsule after the first fill composition has been put into the capsule but before the addition of the second fill composition so as to form an effective barrier between the two compositions.
If the capsule is required to contain more than two fill compositions then layers of the barrier material can be added to the capsule between additions of the different f ll compositions.
Ir. addition, the barrier material must, of course, be physiologically compatible since it is to be included in a pharmaceutical formulation.
Materials which have been found to be particularly useful as barrier materials in capsules are glycerides having a transition temperature (melting point) above 37°C. Ξ-itable glycerides include di- and tri-glycerides, such as many of the various GELUCIRE compounds, which are hyαrogenated fatty acid esters available from Gattefosse.
The word GELUCIRE is a trade mark.) Other trade marks cf suitable glycerides include LABRAFIL and PRECIROL. GΞLUCIRE compounds and other suitable compounds having transition temperatures of from 40°C to 70°C are preferred. Specific examples of exemplary GELUCIRE compounds, and their equivalents include:
GELUCIRE 44/14
GΞLUCIRE 50/02
GELUCIRE 50/13
GELUCIRE 54/02 (also available as PRECIROL)
GELUCIRE 62/05 and GELUCIRE 64/02 (also available as PRECIROL WL 2155) .
The first two digits in the numeric portion of the
GΞLUCIRE name represent the liquid/solid phase transition temperature in degrees centigrade and the second two digits represent the hydrophile/lipophile balance (HLB) value.
Z-ΞLUCIRE 44/14 has a high HLB value and is therefore relatively hydrophilic. This means that it is particularly useful as a carrier m capsules containing lipopmlic fill compositions sucn as those αescriceα m WO-A-9206680 since it will ce immiscible with both of the f ll compositions.
The other compounds are more suitable for use in capsules with a hydrophilic fill since tney are all relatively lipopmlic .
A furtner use for the nydropmlic phase barrier may be to allow the formulation of a hydrophilic drug for co- admmistration with the lipophilic delivery system described m WO-A-9206680. An example of this application is the formulation and delivery of a non- memcrane damaging Pile acid (a nydrophilic material) as descnced m WO-A-9325192 together with a lipophilic drug m the lipophilic delivery system described in WO-A- 9206680. The advantage cf this arrangement is for the improved delivery of drugs which undergo botn high hepatic first-pass metapolism and enterohepatic recycling •. e . g . naloperidol, cnlorpromazme and morphine) or where tne non-membrane damaging bile acid can attenuate the toxic effects of a drug subject to high first-pass metapolism and formulated as described m WO-A-9206680.
Conversely, where a lipopmlic barrier is used to separate hydrophilic phases it may act as a reservoir for a co-administered lipophilic drug.
Another way m which intermixing may be prevented with tne bipnasic rapid ana sustained-release formulations described m WO-A-9206680 containing C12 to C24 fatty acids, is to ensure that tne rapid-release pnase remains a solid at normal storage temperature, e.g. below 30°C. This may ce acmeved by mixing a hydrophobic Gelucire** with a melting point aoove 30°C, exemplified cy Gelucire 33/01, witn the molten rapid release component before filling into capsules, the rapid-release phase solidifying on cooling and thus being unable to undergo mixing with the resident solid sustained-release formulation component. An example of this formulation approach is given celow m Example 3.
If is preferred that hard gelatin capsules are used and, m that case, liquid fill compositions may contain gelatin softening agents such as those described in WO-A- 9102520. Suitable gelatin softening agents can be found by reference to the art of manufacturing soft gelatin capsules where sucn materials are incorporated into the mix which forms the gelatin wall. Particularly suitable gelatin softening agents include glycerol, propylene glycol, glycerol mono-oleate and sorbitol .
The capsules may be enteric coated or otherwise protected to ensure better survival of the pharmaceutically active compound through the stomach. Any convenient enteric protection metnod may be used. Capsules containing the formulation may ce coated with an enteric coat such as hydroxypropyimethylcellulose phthalate or by the commercial coating process of Pharma-Vinci A/S (Denmark) .
The formulations of the invention may be prepared by any suitable process cut when a solid barrier material is used then the process may comprise filling the first fill composition, the carrier material and the second fill composition sequentially into a suitable capsule.
Therefore, m a further aspect of the invention, there is proviαeα a process ror tne preparation of a capsule containing at least two fill compositions separated by a barrier material, the process comprising filling a first fill composition, the carrier material and a second fill composition sequentially into a suitable capsule.
Preferred barrier materials are as described above.
The capsule may be of any suitacle material, for example hard gelatin capsules, soft gelatin capsules and starch capsules out gelatin capsules are preferred, particularly hard gelatin capsules.
The invention will now be further described with reference to the following examples which are not intended to be limiting.
EXAMPLE 1 - Biphasic Pro*pranolol Formulation with Phase Barrier
The following example is a iphasic rapid and sustained- release propranolol formulation similar to that described m WO 92/06680. Typically these materials melt upon neatmg, thereoy allowing tne use of conventional mixing ana pumping technology for fluid filling.
A. Sustained-Release Phase σ/capsule
Propranolol 40.0 Oleic Ac d BP 102.1
Colloidal silicon dioxide (Aerosil 200) 8.2
Polyoxyi-40-hyαrogenated castor oil NF 27.2
^Cremopnor RH40; Saturated polyglycclysed glycerides Ph.F. 94 Geiucire 50/02)
B. Phase Barrier
Saturated polyglycolysed glycerides Ph.F. 150.0 (Geiucire 44/14)
C. Rapid-Release Phase
Propranolol base 40.0 Oleic acid BP 110.0
A. Sustained-Release Phase
The oleic acid, Geiucire 50/02 and Cremophor were heated to 50°C-55°C until a clear solution was obtained. Propranolol base was added with stirring, while maintaining the temperature of the mix at 50°C and continued until the propranolol base was fully dissolved. Finally Aerosil was added while stirring. A total of 272 mg of the formulation was filled into size 0 hard gelatin capsules while hot and then allowed to solidify with cooling.
B. Phase Barrier
The Geiucire 44/14 was heated until fully melted at 45°C-55°C and 150 mg filled over the sustained- release phase, previously filled into size 0 hard gelatin capsules, and allowed to solidify with cooling. C. Rapid-Release Phase
Oleic acid was heateα witn stirring at 45°C-50°C. Propranolol base was added and dissolved with stirring and allowed to cool. A total of 150 mg of the liquid rapid-release formulation was then filled over the phase barrier. The resulting capsules contained a solid sustained-release phase, solid phase separation barrier and liquid rapid-release phase. The capsules were then sealed by gelatin banding. Following gelatin banding, the capsules may be enteric-coated as described in WO 92/06680.
EXAMPLE 2 - Dissolution Studies With and Without Phase Barrier System
For evaluating the dispersion behaviour of the experimental formulations, a test-method was devised based upon the USP XXII dissolution test for tablets and capsules. The aim of the test was to subject the samples to an environment similar to that in the intestine. Dispersion in 5 nours was selected as a satisfactory total release time for the test samples. This was based on the understanding that lympnatic absorption occurs predominantly m the small intestine.
The dissolution apparatus as specified by the USP XXII (apparatus 2) was used with Sorensens phosphate buffer, pH 6.8 containing 0.2% sodium cholate and 0.1% sodium deoxycholate, equilibrated to 37°C. The total volume of buffer added to each dissolution vessel was 900 ml, with a paddle rotation speed of 70 rpm. The paddle height was aαiusted so that tne top edge of the blade was level with tne surface of the liquid. The test sample was dropped ιnto Hi-issoiution medium and the rotation of the paddle started. The test sample was allowed to float freely at the liquid surface throughout the test. At each time-point, a 5 ml aliquot of the dissolution medium was removed and replaced with 5 ml of fresh buffer solution. Each 5 ml sample was initially filtered through a 1.2 μM coarse filter and subsequent 1.2 μM fine filter. The absorbance of the filtered solution was then determined at 290nm using a UV at 290 nm using a UV spectrophotometer. The propranolol concentration in the dissolution medium was calculated using a pre-determined calibration curve for propranolol.
A = Example 1 with phase barrier. B = Example 1 without phase barrier,
Table 1 30°C Storage
% Propranolol Release
Time Initial 3 Months 7 Months (minutes)
A B A B A B
36 44 39 30 34 23
30 41 53 38 45 29
60 49 60 57 47 50 35
120 58 64 64 61 55 43
300 77 71 78 71 69 59 Table 37°C Storage
% Propranolol Release
Time Initial 1 Month (minutes)
A B A B
15 36 44 26 15
30 41 53 44 25
60 49 60 48 37
120 58 64 51 45
300 77 71 62 54
As is clear from the results shown in Tables 1 and 2 the presence of a barrier between the solid sustained release phase and the liquid phase improves considerably the amount of propranalol released, particularly from the sustained release phase. The effect of the barrier increases with the length of time for which the capsules are stored.
EXAMPLE 3 - Biphasic Propranolol Formulation with Solid Rapid-Release Phase
This is an example of a biphasic rapid and sustained- release propranolol formulation based on that described in WO-A-9206680, except that phase intermixing is prevented by having a solid rapid-release phase. The rapid-release phase is formulated as a solid, using Geiucire*3' 33/01, which melts on heating above 30°C allowing (i) capsule filling to take place using conventional mixing and pumping technology, and (ii) 1 A
enables rapid-release to take place at normal temperature .
A. Sustained-Release Phase mσ/capsule
As for Example 1 272.0
B. Solid Rapid-Release Phase
Propranolol base 40.0
Oleic acid B.P. 110.0
Saturated polyglycolysed glycerides Ph.F. 150.0 (Geiucire® 33/01)
The modified rapid-release phase was manufactured by heating cieic acid at 45-50°C with stirring. Propranolol base and Geiucire® 33/01 were added with stirring until completely dissolved. The molten rapid-release phase was maintained above 37°C until filled into capsules already containing the solid sustained-release phase described in Example 1. A total of 300 mg of the modified sustained- release phase containing Geiucire® 33/01 was filled into size 0 hard gelatin capsules while hot and then allowed to solidify with cooling. The capsules were then sealed by gelatin banding. Following gelatin banding, the capsules may be enteric-coated as described in WO-A- 9206680 and Burns et al , International Journal of Pharmaceutics, 110: 291-296 (1994) . EXAMPLE 4 - Dissolution Studies Using Solid Rapid-Release Phase System
The same dissolution method as described in Example 2 was used to evaluate capsules containing the biphasic rapid and sustained-release preparation described in Example 3.
Table 3 - 25°C Storage
% Propranolol Release
Time Initial 2 Months 12 Months (minutes)
15 32 26 23
30 52 49 50
60 60 61 64
120 65 67 71
300 75 83 82
Table 4 30°C Storage
% Propranolol Release
Time Initial 1 Month 2 Months 12 Months (minutes)
15 32 22 27 14
30 52 43 54 37
60 60 59 62 66
120 65 64 80 76
300 75 84 85 77 The results m Table 3 show that at 25°C the dissolution profile cf a c pnasic formulation is maintained for at least 12 months. Table 4 shows that at 30°C, close to the melting point of the modified rapid-release phase containing Geiucire® 33/01, there is a small deterioration m initial release rate. However, the overall biphasic release characteristics of the formulation are maintained.

Claims

1. A pnarmaceutical formulation comprising a capsule containing at least two fill compositions, characterised in that tne compositions are prevented from mixing with one another.
2. A pnarmaceutical formulation as claimed in claim 1, wherein both of the fill compositions are solid.
3. A pnarmaceutical formulation as claimed in claim 1, wherein the two fill compositions are separated by a physical barrier.
4. A formulation as claimed n claim 3, wherein the barrier is of the same material as the capsule.
5. A formulation as claimed m claim 3, wherein the barrier comprises a material r.avmg a melting point higher tnan 25°C.
6. A formulation as claimed m claim 5, wherein the barrier comprises a material having a melting point of higner than 37°C.
7 A formulation as claimed m any one of claims 3 to 6, wherein the fill compositions are hydrophobic m nature and the barrier comprises a hydrophilic material.
8. A formulation as claimed n any one of claims 3 to
6, wnerem the fill compositions are hydrophilic in nature and the barrier comprises a hydropnobic material .
9. A pnarmaceutical formulation as claimed in any one of claims 3 to 8, wherein the barrier comprises a glyceπde, for example a di- or tri-glyceride, or a mixture cf glycerides.
10. A composition as claimed m claim 9, wherein the barrier material comprises a hydrogenated fatty acid ester or a mixture of esters, available under one of the following trade marks:
GELUCIRE 44/14
GELUCIRE 50/13
GELUCIRE 50/02
GELUCIRE 54/02 (also available as PRECIROL)
GELUCIRE 62/05 and GELUCIRE 64/02 (also available as PRECIROL WL 2155) .
11. A formulation as claimed in any one of claims 3 to 10 comprising a first fill composition comprising a C12-C24 fatty acid and a pharmaceutically active substance, formulated for non-sustained release on non-parenteral administration; and a second fill composition comprising a C12-C24 fatty acid and a pharmaceutically active substance formulated for sustained release of the active substance on non-parenteral administration.
12. A formulation as claimed in claim 11, wherein the first and the second fill compositions are hydrophobic in nature and tne barrier is formed from a mixture of hydrogenated fatty acid esters sold under the trade mark GELUCIRE 44/14.
13. A formulation as claimed in any one of claims 1 to 6 or any one of claims 8 to 10 comprising a first fill composition comprising a biologically active material and a Pile acid salt and a second fill composition comprising an agent aαapted to adjust the pH of the gut to a pH value of from 7.5 to 9.
14. A formulation as claimed in claim 13 wherein the biologically active material is a protein such as insulin, calcitonm, a growth hormone, an mterferon, an interleukm or an active fragment of any of these.
15. A formulation as claimed in claim 13 or claim 14 wherein the buffering agent comprises carbonate and/or bicarbonate ions .
PCT/GB1994/002703 1993-12-13 1994-12-12 Biphasic capsule formulation Ceased WO1995016438A1 (en)

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AU11967/95A AU702464B2 (en) 1993-12-13 1994-12-12 Biphasic capsule formulation
US08/666,563 US6153218A (en) 1993-12-13 1994-12-12 Biphasic capsule formulation
AT95902878T ATE213406T1 (en) 1993-12-13 1994-12-12 TWO-PHASE COMPOSITION IN CAPSULE FORM
NZ277074A NZ277074A (en) 1993-12-13 1994-12-12 Pharmaceutical capsule comprising two separated compositions
BR9408294A BR9408294A (en) 1993-12-13 1994-12-12 Pharmaceutical formulation
EP95902878A EP0734253B1 (en) 1993-12-13 1994-12-12 Biphasic capsule formulation
DK95902878T DK0734253T3 (en) 1993-12-13 1994-12-12 Two-phase capsule formulation
JP7516594A JPH09506606A (en) 1993-12-13 1994-12-12 Two-phase capsule formulation
DE69429928T DE69429928T2 (en) 1993-12-13 1994-12-12 TWO-PHASE CAPSULE COMPOSITION
CA002179041A CA2179041C (en) 1993-12-13 1994-12-12 Biphasic capsule formulation
US10/652,834 US20050191347A1 (en) 1993-12-13 2003-08-29 Pharmaceutical formulations
US11/734,183 US20070202161A1 (en) 1993-12-13 2007-04-11 Pharmaceutical Formulations

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GB9325445.6 1993-12-13

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AU (1) AU702464B2 (en)
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DE69429928D1 (en) 2002-03-28
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SG64292A1 (en) 1999-04-27
AU702464B2 (en) 1999-02-25
US20070202161A1 (en) 2007-08-30
JPH09506606A (en) 1997-06-30
ZA949931B (en) 1996-06-13
CN1137235A (en) 1996-12-04
US20050191347A1 (en) 2005-09-01
NZ277074A (en) 1998-01-26
BR9408294A (en) 1997-08-26
US6613353B1 (en) 2003-09-02
US6153218A (en) 2000-11-28
DE69429928T2 (en) 2002-11-28
EP0734253A1 (en) 1996-10-02
DK0734253T3 (en) 2002-07-01
AU1196795A (en) 1995-07-03
ES2172576T3 (en) 2002-10-01
GB9325445D0 (en) 1994-02-16
ATE213406T1 (en) 2002-03-15

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