WO2010136952A2

WO2010136952A2 - Self-microemulsifying mitotane composition

Info

Publication number: WO2010136952A2
Application number: PCT/IB2010/052292
Authority: WO
Inventors: Florian Battung
Original assignee: Hra Pharma Llc
Priority date: 2009-05-25
Filing date: 2010-05-24
Publication date: 2010-12-02
Also published as: ES2472424T3; EP2255786A1; WO2010136952A3; JP5572699B2; US20130017258A1; US8486445B2; EP2435022B1; JP2012528141A; BRPI1010563A2; EP2435022A2

Abstract

The invention relates to a self-microemulsifying drug delivery system ("SMEDDS") of mitotane, with enhanced bioavailability. More particularly the invention provides a mitotane oily formulation comprising propylene glycol monocaprylate (10 to 30% w/w), propylene glycol dicaprate (20 to 60% w/w) and polyoxyethylenesorbitanne monooleate (10 to 30% w/w).

Description

Self-microemulsifying mitotane composition

The invention relates to a self-microemulsifying drug delivery system ("SMEDDS") of mitotane, with enhanced bioavailability.

Technical background:

Mitotane (o,p'-DDD or I .i -dichlorodiphenyldichloroethane) is an adrenolytic agent which is particularly useful in the treatment of non-resectable and metastasized adrenocortical carcinoma. However mitotane has poor solubility in gastro-intestinal tract and low bioavailability when administered as a conventional tablet in humans. Attempts were made to solve this problem. A first self-microemulsifying drug delivery system ("SMEDDS") of mitotane was developed, comprising mitotane dissolved in a matrix composed of an equal mixture of capryol®90, Tween®20 and Cremophor EL® (33:33:33) (Attivi et al, "Development of a self-microemulsifying drug delivery system of mitotane (o,p'-DDD) using a mixture design methodology", Chimiometrie 2006, Ajana Imane, 2006, Master "Sciences de Ia vie et de Ia sante", Nancy- Universite). However this system could not load more than 250mg of mitotane in I OOOmg of matrix, which is not enough to produce capsules of an acceptable size and would therefore seriously entail patients' compliance with the treatment. Optimization of this system was thus needed.

Summary of the invention:

The invention provides a delivery system which incorporates high mitotane loads without forming precipitates in the presence of water.

More particularly, the invention provides a mitotane oily formulation which comprises mitotane in a matrix comprising a. propylene glycol monocaprylate; from 10 to 30% of the total weight of the mitotane oily formulation (w/w) b. propylene glycol dicaprate; from 20 to 60% of the total weight of the mitotane oily formulation (w/w) c. polyoxyethylenesorbitanne monooleate. from 10 to 30% of the total weight of the mitotane oily formulation (w/w)

Advantageously, this matrix can accommodate a drug loading of at least 33%, preferably at least 39%.

This oily formulation is capable of forming a microemulsion in situ with the biological fluids of the body.

The invention further provides a pharmaceutical composition comprising such mitotane oily formulation.

This pharmaceutical composition, which is preferably in the form of a capsule, is useful in treating cancer, in particular adrenocortical carcinoma.

Another subject of the invention is a method for preparing a mitotane oily formulation suitable for forming a self-microemulsifying drug delivery system, which method comprises dissolving mitotane in a mixture of propylene glycol monocaprylate, propylene glycol dicaprate and polyoxyethylenesorbitanne monooleate in proportions as recited above.

Detailed description:

Definitions:

The term 'matrix' refers to a mixture of excipients.

The term 'mitotane oily formulation' refers to a matrix in which mitotane has been incorporated. Drug loading corresponds to the weight of mitotane with respect to the total weight of the matrix. (Equation (1 ))

_{^ τ j}. weight of mitotane . .. ._ ,. . . .

Drug Loadmg = - xlOO Equation (1 ) weight of matrix

SMEDDS (self-microemulsifying drug delivery systems) are defined as isotropic mixtures of lipid, surfactant, cosurfactant, and drug that rapidly form a microemulsion when mixed with water. Such systems are described in greater details in Grove and Mϋllertz, "Liquid Self-Microemulsifying Drug Delivery Systems", Oral Lipid-Based Formulations - Enhancing the Bioavailability of Poorly Water-Soluble Drugs, edited by David J. Hauss, lnforma Healthcare, 2007, Chapter 5. Self-emulsifying formulations are readily dispersed in the gastrointestinal tract, where the motility of the stomach and small intestine provides the agitation necessary for emulsification.

In the present mitotane formulation, the lipophilic phase comprises propylene glycol dicaprate, polyoxyethylenesorbitanne monooleate that acts as a surfactant, and propylene glycol monocaprylate that acts as a cosurfactant. Propylene glycol monocaprylate is available under the name Capryol®90 (Gattefosse).

Propylene glycol dicaprate is available under the name Captex®100 (Abitec corp.). Polyoxyethylenesorbitanne monooleate is available under the name Tween®80 (Sigma) or is also known as polysorbate 80 (or "PS 80" in the examples below).

In a particular embodiment, the oily formulation has a drug loading of at least 33%, preferably between 33% and 67%, and more preferably between 37% and 54%.

The mitotane oily formulation comprises a. from 10 to 30 % w/w of propylene glycol monocaprylate, preferably from 15 to 20%, more preferably from 15 to 17% w/w; b. from 20 to 60 % w/w of propylene glycol dicaprate, preferably from 35 to 50%, more preferably from 38 to 42% w/w; c. from 10 to 30 % w/w of polyoxyethylenesorbitanne monooleate, preferably from 15 to 20%, more preferably from 15 to 17% w/w.

The mitotane oily formulation of the invention makes it possible to load at least 33%, preferably at least 39% of mitotane (i.e. 400mg mitotane for I OOOmg of the matrix made of the mixture of lipid, surfactant and cosurfactant). In a preferred embodiment, propylene glycol monocaprylate, propylene glycol dicaprate and polyoxyethylenesorbitanne monooleate represent a total amount of between 65 and 75 % w/w in the mitotane oily formulation. The oily formulation of the invention advantageously forms a microemulsion comprising droplets having a size of less than 200nm, when mixed with water or HCI.

The mitotane oily formulation can be packaged in any pharmaceutical composition for oral administration.

Suitable oral compositions that comprise the oily formulation of the invention are generally capsules, including hard gelatin capsules or soft gelatin capsules. For instance, soft gelatin capsules are made with a gelatin shell, optionally in association with plasticizers such as glycerine and/or sorbitol. Encapsulation is achieved by techniques known in the art.

In another embodiment, the composition may be a liquid dispersed directly into the patient's mouth. The pharmaceutical composition may then comprise water or an aqueous phase, in which the oily mitotane formulation is dispersed in the form of a microemulsion.

In a further embodiment, the mitotane oily formulation may be packaged into a solid dosage form, in a state readily converted to a microemulsion in vivo, which thereby enhances the dissolution of the drug.

The composition of mitotane oily formulation for therapeutic use advantageously contains between 100 and 400 mg mitotane, preferably between 100 and 300mg.

A particular example of a composition according to the invention is a soft gelatin capsule encapsulating an oily formulation comprising from 33% to 66% of mitotane drug load and a matrix comprising : a. propylene glycol monocaprylate: from 15 to 17% of the total weight of the mitotane oily formulation (w/w) b. propylene glycol dicaprate: from 38 to 42% of the total weight of the mitotane oily formulation (w/w) c. polyoxyethylenesorbitanne monooleate: from 15 to 17% of the total weight of the mitotane oily formulation (w/w) The mitotane oily formulation of the invention, which is suitable for forming a self- microemulsifying drug delivery system may be prepared by dissolving mitotane in a mixture of propylene glycol monocaprylate, propylene glycol dicaprate and polyoxyethylenesorbitanne monooleate in proportions as recited above.

Drug loading of at least 33%, preferably at least 39%, can be achieved by immediate dispersion upon dilution into a homogenous solution.

If desired, the dissolution step may also be carried out by mixing for at least 5 minutes with heating to not more than 40-50⁰C.

The SMEDDS system of the invention enhances the dissolution of mitotane, and its bioavailability. Further food effect is reduced.

The examples and figures illustrate the invention without limiting its scope.

Legends to the figures:

Figure 1 is a graph that shows relative bioavailability vs lysodren (LYSO= Lysodren. Absorption of Lysodren is set as 100%).

Figure 2 is a graph that shows mitotane rate of absorption in fed conditions.

Examples:

Example 1 : Screening of mitotane SMEDDS formulations

Various SMEDDS formulations were screened for drug solubility, stability, and water tolerance.

Solubility was determined by incremental loading of mitotane. A typical increment solubility study is summarized below:

One gram of vehicle was weighed into a 5mL glass vial. Mitotane was added in increments of 10 to 20mg. The contents were mixed. If mitotane dissolved (yielding a clear solution) another increment of mitotane was added. If mitotane did not dissolve, the contents were mixed for at least 5 minutes with heating to not more than 45°C ± 5°C. Clarity of the solution was visually determined after each addition. Clear drug solutions were stored at room temperature for 24 hours and were then re-evaluated for clarity. The increments of mitotane added that produced a clear solution were summed, and this solubility was reported. A visual description of the material after the addition of the final increment was also noted. Due to the drug precipitation overnight in some samples, selected systems were tested at 50% and 55% drug loading in a direct loading solubility study. A direct loading solubility study is summarized below:

One gram of vehicle was weighed into a 5ml_ glass vial. The full amount of Mitotane was added in a single portion. The contents were heated to 45°C ± 5°C and mixed for at least two hours; during this time clarity was assessed every thirty minutes. Drug solutions were then stored at room temperature for 24 or 48 hours and were re-evaluated for clarity.

Stability was determined by placing the systems in a refrigerator (5°C) or left at room temperature. At a minimum of 24 hours, solutions were visually evaluated. Any precipitate was noted.

Since water migration often occurs during manufacturing of soft gelatin capsules, a water uptake study was performed to evaluate the stability of mitotane solutions during the encapsulation and drying processes. Mitotane oily formulation and matrix were tested. The water uptake study was performed as follows: - 3.Og of mitotane oily formulation (with 50% drug loading) was weighed into a scintillation vial;

- 300 mg of water (10%w/w of mitotane oily formulation) was weighed and placed in the vial and then vortex mixed for a minimum of 5 minutes;

- clarity of solution was visually determined; - if the solution was clear, an additional 300 mg of water was added (to bring the total added water to 20%w/w) then vortex mixed for a minimum of 5 minutes;

- clarity of mixture was visually determined. Microemulsions comprising droplets of a size inferior to 200nm appear as clear solutions. Any hazy appearance or precipitate is noted.

Water tolerance study further allows to determine whether the system will self- emulsify in the presence of gastro-intestinal fluid in vivo, for instance.

Table 1 shows formulations with the best drug loading, which were selected for further studies.

Prior art formulation from Attivi et al, 2006, supra, is included in Table 1 , for comparison purposes.

Formulations numbered 1 to 4 were eventually set aside, as high mitotane loads could not be incorporated.

Table 1 : Comparative formulations

Table 2 shows the characteristics of the two selected formulations. Table 2: Selected formulations

Example 2: Bioavailability and absorption studies

Formulations #054 and 057 according to the invention (see Example 1 ) were tested in dogs, in a screening study vs. Lysodren® (mitotane tablets commercially available from HRA pharma). Three Beagle dogs/group were used per formulation. One group is administered with one Lysodren tablet comprising 500mg of mitotane, one group is administered with two hard gelatin capsules comprising 280mg mitotane each in formulation #054 and one group is administered with two hard gelatin capsules comprising 280mg mitotane each in formulation #057. The formulations were compared in fed and fasted conditions, including administrations on fed dogs and then fasted dogs in cross over with a wash out period of 3 weeks. 10 samples were collected at: 0, 1 , 2, 3, 4, 5, 6, 8, 10 and 12 hours post administration.

Relative bioavailability data vs Lysodren® are as follows: Lysodren® : 100% Batch # 054 : 150 % Batch # 057 : 317% See Figure 1.

Absorption is slower for the two formulations of the invention (about 8 hours) than for Lysodren® (about 5 hours), which might be explained by an increase of lymphatic absorption. Such slow absorption (vs a mesenteric absorption) is advantageous in that it reduces the variations of absorption which are inherent to the use of mitotane. See Figure 2.

Food effect on mitotane absorption is dramatically reduced with the two formulations of the invention (Lysodren® is substantially not absorbed at all without food). Table 3: Food effect

Example 3 : Manufacturing of mitotane SMEDDS soft gelatin capsules

This example provides a protocol for manufacturing mitotane SMEDDS soft gelatin capsules having the following composition:

Table 4A: Quantitative formula for gel mass (Gel mass Batch size: 250kg): lngredient(s) %w/w

Gelatin USP/NF (150Bloom Limed 42.00 Bone, Type B)

Glycerin, USP 99.7% 3.00

Sorbitol Special 18.00

Purified water, USP 34.92

Opatint White (G-18000) 2.00

FD&C BIue # 1 0.08

TOTAL 100.0

Table 4B: Quantitative formula for capsule

Brief manufacturing procedure : Fill material:

1. Charge the Capryol 90 into a container equipped with an overhead mixer.

2. Mix to create a vortex

3. Charge Captex 100 into the mixing Capryol 90. Mix until homogenous solution is obtained. 4. Charge Polysorbate 80, mix until a homogenous solution is obtained.

5. Heat to 45°C ± 5°C. 6. Once the temperature is in the above mentioned range, slowly charge the mitotane into the mixing solution. Mix until mitotane is completely dissolved into solution.

7. Deaerate final solution.

Gelatin Mass:

1. Reserve approximately 1 liter of water. Charge remaining purified water, USP, into gelatin melter and adjust the temperature to 90⁰C.

2. Charge sorbitol special and glycerine, USP 99.7%. 3. Charge Gelatin and heat to 80⁰C under continuous mixing until gelatin granules are completely dissolved.

4. In a separate pot, charge colorants. Mix until a homogeneous suspension is obtained.

5. Charge step 4 into step 3 under continuous mixing. 6. Rinse step 5 container with the reserved purified water and charge into step

3. Mix until a homogenous gel mass is obtained. 7. Deaerate the gel mass (air vacuum adjusted to 25-30 in Hg).

Encapsulation and processing: 1. Carry out the encapsulation

2. Tumble-dry the capsules

3. Tunnel -dry the capsules

Claims

1. A mitotane oily formulation comprising mitotane in a matrix comprising a. from 10 to 30 % w/w of propylene glycol monocaprylate; b. from 20 to 60 % w/w of propylene glycol dicaprate; c. from 10 to 30 % w/w of polyoxyethylenesorbitanne monooleate.

2. The oily formulation of claim 1 , comprising at least 33% drug load of mitotane.

3. The oily formulation of claim 1 , comprising at least 39% drug load of mitotane.

4. The oily formulation of claim 2, comprising between 33% and 66% drug load of mitotane.

5. The oily formulation of claim 4, comprising between 37% and 54% drug load of mitotane.

6. The oily formulation of any of claims 1 to 5, wherein propylene glycol monocaprylate, propylene glycol dicaprate and polyoxyethylenesorbitanne monooleate represent a total amount of between 65 and 75 % w/w of the mitotane oily formulation.

7. The oily formulation of any of claims 1 to 6, which forms a self- microemulsion comprising droplets having a size of less than 200nm when mixed with water or HCI.

8. A pharmaceutical composition, comprising the oily formulation as defined in any of claims 1 to 7.

9. The composition of claim 8, which is in a form suitable for oral administration.

10. The composition of claim 9, which is a capsule.

11. The composition of claim 10, which is a soft gelatin capsule.

12. The composition of claim 9, comprising between 100 and 400 mg mitotane.

13. The composition of claim 11 , which is a soft gelatin capsule encapsulating an oily formulation comprising from 33 to 66% of mitotane drug load and a. from 15 to 17 % w/w of propylene glycol monocaprylate; b. from 38 to 42 % w/w of propylene glycol dicaprate; c. from 15 to 17 % w/w of polyoxyethylenesorbitanne monooleate.

14. The composition of any of claims 9 to 13, for use in treating cancer.

15.A method for preparing a mitotane oily formulation suitable for forming a self-microemulsifying drug delivery system, which method comprises dissolving mitotane in a mixture of propylene glycol monocaprylate, propylene glycol dicaprate and polyoxyethylenesorbitanne monooleate in proportions as recited in claim 1.