US20040214320A1

US20040214320A1 - Mammalian gamete and embryo culture media supplement and method of using same

Info

Publication number: US20040214320A1
Application number: US10/764,821
Authority: US
Inventors: David Gardner; Michelle Lane
Original assignee: Vitrolife Inc
Current assignee: Vitrolife Inc
Priority date: 2000-06-09
Filing date: 2004-01-26
Publication date: 2004-10-28
Also published as: EP1287119B1; WO2001094552A3; BR0111537A; JP4202121B2; CN1250712C; CA2410931A1; ATE532855T1; DK1287119T3; JP2003535585A; CA2410931C; KR100736422B1; US20020042132A1; NZ523481A; HK1059454A1; ES2377194T3; EP2228439A1; EP1287119A2; CN1446256A; WO2001094552A2; AU6830801A

Abstract

The present invention provides a supplement and a culture media useful for culturing mammalian gametes and embryonic tissue. The culture media comprises at least one of recombinant human albumin, fermented hyaluronan, and citrate. Because the constituents are produced from non-conventional sources, the culture medium is free from contaminants such as viruses, prions and endotoxins. Additionally, because the medium is completely defined, the medium is not subject to variations which can impair the development of mammalian cells and prevent meaningful comparisons of empirical studies.

Description

CROSS-REFERENCE TO RELATED APPLICATION

This application is a continuation of U.S. patent application Ser. No. 09/877,395, filed Jun. 8, 2001, which claims priority from U.S. provisional patent application No. 60/210,649, filed Jun. 9, 2000, and from U.S. provisional patent application No. 60/212,232, filed Jun. 16, 2000.[0001]

FIELD OF THE INVENTION

The present invention relates to culture media which provide useful environments for cellular development. More particularly this invention relates to defined culture media supplement containing constituents produced from non-traditional sources that, when added to culture media, avoid the problems of prior culture media.

BACKGROUND OF THE INVENTION

For years media supplements for culturing mammalian embryonic cells have been derived from animal fluids, and in particular blood serum. While serum based media supplements have been somewhat effective for culturing certain types of cells and tissues, these media supplements have been found to be undesirable. One of the main reasons that these serum based media supplements are unattractive candidates for culturing cells is because of the possibility that the resulting media will contaminated with impurities, toxins, and infective agents found in the fluid from which the media is derived. Additionally, because the animals from which the blood is collected are different and live in differing environments, the fluids produced by these animals have different components at differing concentrations. One important aspect of serum based medium that has been recognized is the requirement of macromolecules in the medium. In an attempt to mimic serum based products, researchers have attempted to add synthetic macromolecules, such as polyvinyl alcohol, to replace the macromolecules in the serum, such as albumin. However, because serum is largely undefined chemically, removing the serum from culture media and attempting to replace only the larger molecules has produced culture media which are less than ideal or ineffective for many purposes because the media are missing essential components.

Accordingly, there is a need for culture media supplements which are as effective as culture media supplements based on blood products while at the same eliminating potential sources of contamination. Additionally there is a need for standardized culture media.

SUMMARY OF THE INVENTION

The present invention describes a novel, physiologically based completely defined supplement to culture media for mammalian embryonic cells and gametes. This medium supplement may be used with in vitro fertilization media, embryo transfer media and embryo cryopreservation media for the mammalian preimplantation embryo, as well as a supplement to media for the development of embryonic stem cells, or any other similar media well known in the art. This supplement contains recombinant human albumin (rHA), fermented hyaluronan (HYN) and/or citrate, and combinations thereof. Addition of this supplement to the culture medium results in equivalent development compared to media supplemented with serum albumin purified from blood.

DETAILED DESCRIPTION OF THE INVENTION

The supplement may comprise recombinant human albumin (rHA) at any appropriate concentrations for the media in which it is to be used. As further described herein, the use of rHA rather than naturally occurring human serum albumin (HSA) has numerous advantages. [0006]
Typically, when the supplement comprises rHA, the supplement comprises between about 0.1 mg/ml to about 20.0 mg/ml of rHA based on the total volume of the medium to which the supplement is added. In one embodiment, about 0.5 mg/ml to about 5.0 mg/ml of rHA is added based on the total volume of the medium. [0007]
The efficacy of the supplement can be enhanced by adding fermented hyaluronan (HYN) to the supplement. The addition of the fermented HYN to the media supplement demonstrates positive results. [0008]
The phrase “increases the viability of gametes or embryonic cells” as used herein is defined as including the increased development of the embryos to the blastocyst stage in the culture, the ability to hatch from the zona pellucida is increased in vitro, and/or an increase in the overall viability of the embryo in embryo cultures when embryos are cultured in a medium containing the supplement of the present invention as compared to being cultured in the same medium without the supplement. [0009]
Furthermore, the addition of fermented HYN to the appropriate medium significantly affects the ability of the blastocysts to survive freezing. The use of fermented HYN has several advantages over the use of HYN from a naturally occurring warm blooded vertebrate source such as purified from rooster comb or umbilical cord. By utilizing fermented HYN rather than HYN from a warm blooded vertebrate source, the ability to control the safety and stability of the HYN from different sources and batches is greatly increased. [0010]
When present, the amount of fermented HYN will generally be at concentrations between about 0.1 mg/ml to about 5.0 mg/ml based on the total volume of the medium. In one embodiment the fermented HYN will be added to the medium at concentrations between about 0.125 mg/ml to about 1.0 mg/ml based on the total volume of the medium. [0011]
The supplement can be further augmented by the addition of citrate. In one embodiment, citrate and rHA are both added to the medium supplement, as it has been surprisingly and unexpectedly discovered that the addition of citrate to a medium supplement containing rHA allows the rHA to closely duplicate the properties of HSA or bovine serum albumin (BSA). The addition of the citrate has a further enhancing effect on the development of the cultured cellular material. Any citrate used for media that is well known in the art may be used, including, but not limited to, choline citrate, calcium citrate, citric acid, sodium citrate, and combinations thereof. In one embodiment, sodium citrate is used. The citrate is generally added at concentrations between about 0.1 mM and about 5.0 mM, based on the total volume of the medium. In one embodiment, the citrate is added at concentrations between about 0.1 mM and about 1.0 mM, based on the total volume of the medium. [0012]
The medium supplement of the present invention comprises rHA, fermented HYN and/or citrate in any useful combination. In one embodiment, the medium supplement, and the medium to which the medium supplement is added, is free from non-recombinant macromolecules or macromolecules purified from an animal source. In another embodiment, the medium supplement, and the medium to which the medium supplement is added, is free of non-recombinant HSA and/or non-fermented HYN. [0013]
This invention is directed to the medium supplement described above, media containing the medium supplement, a method of making the medium supplement, kits containing the medium supplement, and a method of growing embryonic material employing the medium supplement described herein. [0014]
The present invention includes a method of growing cellular material, in one embodiment embryos, employing the medium supplement described herein such that they can be included in medium at the start of culture, or can be added in a fed-batch or in a continuous manner. Moreover, the components of the medium supplement may be added together, or separately, at different stages of the media production. [0015]
This supplement can be added to any appropriate mammalian cellular material culture media well known in the art, including but not limited to, embryo culture media, embryo transfer media and embryo cryopreservation media (to include both freezing and vitrification procedures) for embryos from any mammalian species, and stem cell media. Any media that can support embryo or cell development could be used, which includes, by way of example only, bicarbonate buffered medium, Hepes-buffered or MOPS buffered medium or phosphate buffered saline. Examples of media are G1.2/G2.2, KSOM/KSOMaa, M16, SOF/SOFaa, MTF, P1, Earle's, Hams F-10, M2, Hepes-G1.2, PBS and/or Whitten's. (Gardner and Lane, 1999; Embryo Culture Systems; Handbook of In Vitro Fertilization, CRC Press, Editors: Trounson AO and Gardner DK, 2[0016] ^ndedition, Boca Raton, pp205-264.)
The production of rHA is well known in the art. In one embodiment, rHA is obtained from genetically modified yeast which produce a human albumin protein. One such methodology for the production of rHA from yeast is taught in U.S. Pat. No. 5,612,197. [0017]
Fermented hyaluronan (HYN) is obtained by any process well known in the art. One such process is the continuous bacterial fermentation of [0018] Streptococcus equi. Hyaluronan is a naturally occurring polymer of repeated disaccharide units of N-acetylglucosamine and D-glucuronic acid. It is widely distributed throughout the body. Typically, the molecular weight of the fermented HYN is 2.3×10⁶kD. The production of HYN from Streptococcus is well known in the art, and any well known process can be used, including those disclosed in Cifonelli JA, Dorfman A. The biosynthesis of hyaluronic acid by group A Streptococcus: The uridine nucleotides of groups A Streptococcus. J. Biological Chemistry 1957; 228: 547-557; Kjems E, Lebech K. Isolation of hyaluronic acid from cultures of streptococci in a chemically defined medium. Acta Path. Microbiol. Scand. 1976 (Sect. B); 84: 162-164; and Markovitz A, et al. The biosynthesis of hyaluronic acid by group A Streptococcus. J. Biological Chemistry 1959; 234(9): 2343-2350.
Other compounds may be added to the medium supplement of the present invention. These include growth factors, as mammalian embryos and cells typically have many receptors for growth factors and the addition of such growth factors may increase the growth rate of the cultured material. Such growth factors include, but are not limited to, Insulin, typically in amounts of 0.1-100 ng/ml; IGF II, typically in amounts of 0.1-100 ng/ml; EGF, typically in amounts of 0.1-100 ng/ml; LIF, typically in amounts of 5-1000 U/ml; PAF, typically in amounts of 0.1-500 μM; and combinations thereof. All amounts are based on the total volume of the media to which the medium supplement is added. [0019]
Medium supplement can be prepared in 2 ways, either as a separate medium supplement that is added to the media after media preparation, or the ingredients of the medium supplement can be added directly to the culture media during media preparation. [0020]
By way of example only, the medium supplement may be prepared on its own as follows. Medium supplement rHA may be made into a stock solution by adding either water, saline or medium to make a concentrated stock solution of between 50-500 mg/ml, usually 250 mg/ml. Alternatively, the solution can be obtained as a 250 mg/ml stock solution. Fermented HYN is reconstituted in water, saline or medium, to make a concentrated stock solution of between 10-500 mg/ml, usually 500 mg/ml. This is achieved by adding the water, saline or medium to a flask and adding the desired amount of HYN to the solution. The HYN is then dissolved by rigorous shaking or mixing using a stir bar. For a 500 mg/ml solution, 500 mg of HYN can be added to 1 ml of solution. Citrate is prepared as a stock solution by adding either water, saline or medium to make a concentrated stock solution of between 5-500 mM, usually 500 mM. For a 500 mM stock solution, 0.9605 g of citric acid is added to 10 ml of solution. The rHA, fermented HYN and citrate stocks are added together to make a single supplement solution that is added to the final medium as a 100× times concentrated stock. For 10 ml of medium, 100 μl of the supplement is added. [0021]
rHA can be added directly to the culture medium as either a powder or as a stock solution. The following embodiment is presented by way of example only. The stock solution may added as 100 μl of 250 mg/ml stock to 9.9 mls of medium. Fermented HYN may be added directly to the culture medium as either a powder or as a stock solution. As a powder, 1.25 mg of HYN may be added to 10 ml of medium. Alternatively, a 125 μl of a 1% stock solution may be added to 9.9 ml of medium. Citrate may be added directly to the culture medium as either a powder or as a stock solution. As a powder, 9.6 mg may be added to 100 mls of medium, or alternatively, 100 μl of a 50 mM stock may be added to 9.9 ml of medium. [0022]
All patents and publications cited herein are hereby incorporated by reference. [0023]
All ranges recited herein include all combinations and subcombinations included within that range limits; therefore, a range from “about 0.1 mg/ml to about 20.0 mg/ml” would include ranges from about 0.125 mg/ml to about 11.5 mg/ml, about 1.0 mg/ml to about 15.0 mg/ml, etc. [0024]
The medium supplement of the present invention solves several problems that persist in the art of culturing mammalian cells, tissues, embryos and other related cellular material. One problem with current media is that the cultured mammalian cellular material, particularly embryos, may become contaminated by contaminants such as prions and/or endotoxins found within macromolecular blood products such as human albumin. An advantage of the supplement of the present invention is that it eliminates the potential contamination associated with the use of blood products in media for culturing embryo and other mammalian cellular materials. [0025]
Another problem with current media is the difficulty in standardizing such media when using blood products such as serum albumin or other naturally occurring materials. Furthermore, the present invention makes it easier to purify the final cultured product, when the naturally occurring variations and contaminants within the blood products in the media are eliminated. [0026]
The present invention eliminates the inherent variation involved when using a biological protein which is often contaminated with other molecules and which differs significantly between different preparations and also between batches within the same preparation. Therefore, the use of recombinant molecules such as rHA enables the formulation of physiological media to be prepared in a standardized fashion. These preparations are endotoxin free, free of prions and are more physiologically compatible than media which are currently used. Current media contain other synthetic macromolecules, such as polyvinyl alcohol or polyvinyl pyrrolidone, which are unable to perform essential physiological functions, such as bind growth factors, and therefore the use of these media result in inferior development of mammalian cellular material. [0027]
The invention will be better understood from the Examples which follow. However, one skilled in the art will readily appreciate that the specific compositions, methods and results discussed are merely illustrative of the invention and no limitations on the invention are implied. [0028]

EXAMPLES

Example 1

Media G1.2/G2.2 were prepared from concentrated stock solutions as shown below in Table 1. rHA was added as a 250 mg/ml stock solution of 200 μl to 9.8 mls of media. Initial experiments have investigated replacing albumin purified from blood with the rHA for outbred mouse embryo development in culture. Fertilized eggs were cultured for 4 days in one of 3 different concentrations of rHA. Embryos were cultured at 37° C. in 6% CO ₂:5% O₂:89% N₂in an embryo incubation volume of 10 embryos: 20 μl of medium. Embryos were cultured in medium G 1.2 for 48 h followed by 48 h of culture in medium G 2.2. The negative control treatment was no protein, the positive control treatment was 5 mg/ml HSA (blood product). The results are shown below in Table 2.

TABLE 1


			G1.2	G2.2	FG1
Stock	Expires	Components	(g/L)	(g/L)	(g/L)

A × 10	3 months	NaCl	5.26	5.26	5.844
conc		KCl	0.41	0.41	0.41
		NaH₂PO₄—H₂O	0.035	0.035	0.078
		MgSO₄—7H₂O	0.246	0.246	0.246
		Na Lactate	1.17	0.66	0.58
		Glucose	0.09	0.568	0.567
		Penicillin	0.06	0.06	0.06
B × 10	1 week	NaHCO₃	2.101	2.101	2.1
conc		Phenol Red	0.001	0.001	0.001
C × 100	2 weeks	Pyruvic Acid	0.0352	0.011	0.0352
conc
D × 100	1 month	CaCl₂—H₂O	0.265	0.265	0.265
conc

G × 100	3 months	alanyl-Glutamine	0.108		0.217		—
conc

T × 100	3 months	Taurine	0.0125		—	0.0125
conc

ED	1 month	EDTA	0.029		—	—
		NaOH solution	0.4

N × 100		Non-Essential Amino	10	ml	10	ml	10	ml
soln		Acids

E × 50		Essential Amino	—	20	ml	—
soln		Acids

V × 100

Vitamins

—

10

ml

soln	10	mls

Stock A and B [0030]
1. Weigh out individual components into a 100 ml flask. [0031]
2. Add 50 ml of H[0032] ₂O (either Extreme H₂O or Biowittaker).
3. Mix well until all components are dissolved. [0033]
4. Add a further 50 ml of H[0034] ₂O.
5. Mix well. [0035]
6. Filter through 0.2 μm filter. [0036]
7. Store at 4 degrees Celsius. [0037]
Stock C-T [0038]
1. Weigh component into a 10 ml tube. [0039]
2. Add 10 ml of H[0040] ₂O (either Extreme H₂O or Biowittaker).
3. Mix well until dissolved. [0041]
4. Filter through 0.2 μm filter. [0042]
5. Store at 4 degrees Celsius. [0043]
Embryo Culture Media Preparation—Part I [0044]
Stock EDTA [0045]
1. Weigh 0.029 g of EDTA into a 10 ml tube. [0046]
2. Weigh 0.4 g of NaOH into a separate 10 ml tube. [0047]
3. Add 10 ml of H[0048] ₂O (either Extreme H₂O or Biowittaker) to NaOH and mix until dissolved.
4. Add 220 μL of NaOH solution to EDTA. [0049]
5. Mix until dissolved. [0050]
6. Add 9.8 ml of H[0051] ₂O to the EDTA.
7. Add 90 ml of H[0052] ₂O to a 100 ml flask.
8. Add 10 ml of EDTA solution to the 90 ml of H[0053] ₂O.
9. Filter through 0.2 μm filter. [0054]

10. Store at 4 degrees Celsius.

TABLE 2


			Cell	ICM	TE	%
rHA mg/ml	Blastocyst	Hatching	Number	Number	Number	ICM/Total

0	76.7	31.7	60.8 ± 2.2^a	13.8 ± 0.7^a	47.1 ± 2.0^a	23.0 ± 0.9
1.25	70.7	46.6	72.6 ± 2.2^bc	17.7 ± 0.6^b	56.4 ± 1.9^bc	24.0 ± 0.6
2.5	75	39.3	78.1 ± 2.5^b	18.4 ± 0.5^b	58.4 ± 2.1^b	24.2 ± 0.5
5	76.8	37.5	65.9 ± 2.7^ac	16.3 ± 0.7^b	49.6 ± 2.4^ac	25.2 ± 0.7
HSA 5 mg/ml	72.6	38.7	74.3 ± 2.4^bc	17.2 ± 0.7^b	56.2 ± 2.0^bc	23.6 ± 0.6

rHA was able to replace HSA for embryo development in culture for at least concentrations of 1.25 to 2.5 mg/ml. [0056]

Example 2

Media G1.2/G2.2 were prepared from concentrated stock solutions as taught in Example 1. Fermented HYN was added from a x100 stock solution of 100 μl to 10 mls of media. [0057]

Initial experiments investigated replacing albumin purified from blood with HYN for outbred mouse embryo development in culture. Fertilized eggs were cultured for 4 days in one of 4 different concentrations of HYN. Embryos were cultured at 37° C. in 6% CO ₂:5% O₂:89% N₂in an embryo incubation volume of 10 embryos: 20 μl of medium. Embryos were cultured in medium G1.2 for 48 h followed by 48 h of culture in medium G2.2. The negative control treatment was no protein. The results are shown below in Table 3.

TABLE 3


HYN			Cell	ICM	TE	%
(mg/ml)	Blastocyst	Hatching	Number	Number	Number	ICM/Total

0	82.4^a	38.3^a	67.3 ± 2.8^a	16.1 ± 0.7^a	50.3 ± 2.3^a	24.6 ± 0.8^a
0.125	88.6^a	57.1b^c	79.6 ± 1.9^bc	21.2 ± 0.8^bc	58.7 ± 1.5^bc	26.5 ± 0.6^ac
0.25	94.5^a	72.7^c	74.9 ± 3.4^bc	21.8 ± 1.2^bc	51.9 ± 2.8^ac	29.7 ± 0.8^bc
0.5	100^a	50^b	64.2 ± 1.9^ac	18.0 ± 0.7^ac	46.7 ± 2.0^a	28.3 ± 1.1^bc
1	61.8^b	23.5^a	62.0 ± 2.7^ac	17.5 ± 0.8^ac	49.1 ± 2.5^a	26.4 ± 0.9^ac

Fermented HYN at least of concentrations from 0.125 to 0.5 mg/ml stimulated mouse embryo development. [0059]

Example 3

Media G1.2/G2.2 were prepared from concentrated stock solutions as taught in Example 1. rHA was added as a 250 mg/ml stock solution of 200 μl to 9.8 mls of media, fermented HYN was added from a x100 stock solution of 100 μto 10 mls of media. Subsequent experiments investigated replacing albumin purified from blood with rHA together with fermented HYN for outbred mouse embryo development in culture. Fertilized eggs were cultured for 4 days. Embryos were cultured at 37° C. in 6% CO ₂:5% O₂:89% N₂in an embryo incubation volume of 10 embryos: 20 μl of medium. Embryos were cultured in medium G 1.2 for 48 h followed by 48 h of culture in medium G 2.2. The results are shown below in Table 4.

TABLE 4


	Cell	ICM	TN
Treatment	Number	Number	Number	% ICM/Total

5 mg/ml HSA	73.3 ± 1.7	17.8 ± 0.6	55.5 ± 1.3	24.3 ± 0.5
1.25 mg/ml rHA +	71.8 ± 1.6	18.6 ± 0.5	53.2 ± 1.3	26.0 ± 0.5*
0.125 mg/ml HYN

Culture with rHA and fermented HYN together significantly increase the development of the inner cell mass cells (ICM). Since ICM development is linearly related to ability to develop into a viable fetus, an increase in % ICM is likely to mean an increase in viability. [0061]

Example 4

Media G1.2/G2.2 were prepared from concentrated stock solutions as taught in Example 1. rHA was added as a 250 mg/ml stock solution of 200 μto 9.8 mls of media, fermented HYN was added from a x100 stock solution of 100 μl to 10 mls of media. Subsequent experiments investigated replacing albumin purified from blood with rHA together with fermented HYN for outbred mouse embryo development after transfer to recipient mice. Fertilized eggs were cultured for 4 days and then transferred at the blastocyst stage to recipient females. Embryos were cultured at 37° C. in 6% CO[0062] ₂:5% O₂:89% N₂in an embryo incubation volume of 10 embryos: 20 μl of medium. Embryos were cultured in medium G1.2 for 48 h followed by 48 h of culture in medium G2.2. The results are shown below in Table 5.

TABLE 5

Fetal Fetus/

Implantation development implantation

rate (%) (%) site (%) Weight (mg)

HSA 63.3 43.3 68.4 208

rHA and HYN 65.0 46.7 71.8 207
Culture with rHA together with fermented HYN resulted in equivalent fetal development to those embryos cultured in medium supplemented with HSA (blood product). [0063]

Example 5

Media G1.2/G2.2 were prepared from concentrated stock as taught in Example 1. rHA was added as a 250 mg/ml stock solution of 200 μl to 9.8 mls of media, fermented HYN was added from a x100 stock solution of 100 μl to 10 mls of media and citrate was added from a x100 stock solution of 100 μl to 10 mls of media. Experiments were performed to determine whether the further supplementation of rHA and fermented HYN together with citrate increased mouse embryo development in culture. Embryos were cultured from the fertilized egg for 48 h with rHA and HYN in the presence or absence of citrate. Embryos were cultured at 37° C. in 6% CO[0064] ₂:5% O₂:89% N₂in an embryo incubation volume of 10 embryos: 20 μl of medium. Embryos were cultured in medium G1.2 for 48 h. The results are shown below in Table 6.

TABLE 6

Day 3 mean

cell number % 8 cell % compacted

no citrate 6.33 ± 0.17 69.7 7.3

citrate 7.21 ± 0.13* 81.1* 12.2*
The addition of citrate to medium containing rHA and fermented HYN resulted in a significant increase in embryo development. [0065]

Example 6

Media G1.2/G2.2 were prepared from concentrated stock solutions as taught in Example 1. rHA was added as a 250 mg/ml stock solution of 200 μl to 9.8 mls of media, fermented HYN was added from a x100 stock solution of 100 μl to 10 mls of media and citrate was added from a x100 stock solution of 100 μl to 10 mls of media. Experiments were performed to determine whether the further supplementation of rHA and fermented HYN together with citrate increased mouse embryo development in culture. Embryos were cultured from the fertilized egg for 48 h with rHA and HYN in the presence or absence of citrate. Embryos were then transferred to culture medium with or without citrate for a further 48 h. Embryos were cultured at 37° C. in 6% CO[0066] ₂:5% O₂:89% N₂in an embryo incubation volume of 10 embryos: 20 μl of medium. Embryos were cultured in medium G1.2 for 48 h followed by 48 h of culture in medium G2.2. The results are shown below in Table 7.

TABLE 7

Morula/ Total Hatching

Blastocyst Blastocyst (% of Cell ICM TE %

Treatment (%) (%) Total) Number Number Number ICM/Total

−/− 53.9 45.2 13 100.4 28.9 71.5 28.4

+/− 71.3 67.3 16.8 112.6 34.9 77.7 30.7

−/+ 68.5 64.8 23.2 94.8 33.4 61.44 34.5

+/+ 72.7 62.7 18.2 100.7 30.9 69.8 30.4
As can be seen by the results in Table 7, the addition of citrate significantly increased embryo development. [0067]

Example 7

Media G1.2/G2.2 were prepared from concentrated stock solutions as taught in Example 1. rHA was added as a 250 mg/ml stock solution of 200 μl to 9.8 mls of media, fermented HYN was added from a x100 stock solution of 100 μl to 10 mls of media and citrate was added from a x100 stock solution of 100 μl to 10 mls of media. [0068]
Initial experiments in the cow have investigated replacing albumin purified from blood (Bovine serum albumin, BSA) with either rHA or fermented HYN or rHA together with fermented HYN for the development of fertilized eggs in culture. Fertilized eggs were cultured for 6 to 7 days. Embryos were cultured at 38.5° C. in 6% CO[0069] ₂:5% O₂:89% N₂in 500 μl of medium. Embryos were cultured in medium G1.2 for 72 h followed by 72 h of culture in medium G2.2. The results are shown below in Table 8.

TABLE 8

Number of Total Blastocyst Total Blastocyst

Treatment Embryos Day 6 Day 7

BSA 592 30.9^a 36.8

rHA 583 22.1^b 38.4

HYN 549 16.9^b 30.4

rHA + HYN 558 27.8^a 39.1
The combination of both rHA with the fermented HYN produced equivalent embryo development in culture of cow embryos as that obtained in the presence of BSA. [0070]

Example 8

Media G1.2/G2.2 were prepared from concentrated stock solutions as taught in Example 1. rHA was added as a 250 mg/ml stock solution of 200 μl to 9.8 mls of media, fermented HYN was added from a x100 stock solution of 100 μl to 10 mls of media and citrate was added from a x100 stock solution of 100 to 10 mls of media. [0071]

Subsequent experiments in the cow have investigated replacing albumin purified from blood (Bovine serum albumin, BSA) with rHA with or without citrate for the development of fertilized eggs in culture. Fertilized eggs were cultured for 6 to 7 days. Embryos were cultured at 38.5° C. in 6% CO ₂:5% O₂:89% N₂in 500 μl of medium. Embryos were cultured in medium G1.2 for 72 h followed by 72 h of culture in medium G2.2. The results are shown below in Table 9.

TABLE 9


			Day 6 Blastocyst
	Total Blastocyst	Day 6 Blastocyst	Inner Cell Mass
Treatment	Day 6	Cell Number	Cell Number

BSA	40.2	143 ± 6^a	46.2 ± 1.9^a
rHA	36.6	123 ± 7^b	37.9 ± 1.9^b
rHA + citrate	41.4	146 ± 5^a	45.3 ± 1.9^a

Supplementing rHA with citrate resulted in equivalent cow embryo development in culture compared to those embryos cultured in the presence of BSA. [0073]

Example 9

Media G1.2/G2.2 were prepared from concentrated stock solutions as taught in Example 1. rHA was added as a 250 mg/ml stock solution of 200 μl to 9.8 ml of media, fermented HYN was added from a x100 stock solution of 100 μl to 10 ml of media and citrate was added from a x100 stock solution to 10 ml of media. [0074]

Subsequent experiments in the cow have investigated addition of fermented HYN to rHA with citrate for the development of fertilized eggs in culture, and subsequent ability to freeze them. Fertilized eggs were cultured for 6 to 7 days. Embryos were cultured at 38.5° C. in 6% CO ₂:5% O₂:89% N₂in 500 μl of medium. Embryos were cultured in medium G1.2 for 72 h, followed by 72 h of culture in medium G2.2. Blastocysts were either stained for cell numbers or frozen and subsequently thawed to assess survival. The results are shown below in Table 10.

TABLE 10


			Survival and
	Total		Re-expansion
	Blastocyst	Day 7 Blastocyst	Following
Treatment	Day 7	Cell Number	Freezing

BSA	42.3	150 ± 10	38.5^a
rHA + citrate	50.0	134 ± 10	57.1^b
rHA + citrate + HYN	51.1	159 ± 10	80^c

Supplementing medium with rHA, citrate and fermented HYN significantly increased the ability of blastocysts to survive freeing and thawing. [0076]

Example 10

Media G1.2/G2.2 were prepared from concentrated stock solutions as taught in Example 1. [0077]

This experiment investigated the effects of growing CF1 mouse embryos in culture in the presence of rHA and HYN on the ability of the embryos to survive freezing and thawing. CF1 mouse embryos were cultured to the blastocyst stage and development and ability to survive the freezing procedure was assessed.

TABLE 11


	Development			Hatching	Completely
	to the	Blastocyst	Re-expansion	After	Hatched
	Blastocyst	Hatching	After	Freezing	After
Treatment	Stage (%)	Rates (%)	Freezing (%)	(%)	Freezing

HSA	88.2	49.0	76.1	42.9	28.6
HSA + HYN	81.8	43.2	79.5	45.5	29.6
rHA + citrate	85.0	53.4	77.5	57.5*	40.0*
RHA + citrate + HYN	79.0	51.9	83.8	67.6*	51.3*

From these results it can be clearly seen that culture with rHA or rHA with HYN significantly increases blastocyst hatching after thawing compared to blastocysts grown with HSA (P<0.05). [0079]

The ability of the blastocysts to outgrow in culture following cryopreservation was also assessed. The outgrowth of both the ICM and TE was scored between 0-3 where 0 represented no outgrowth and 3 represented extensive outgrowth. Outgrowth has been shown to be related to viability (Lane and Gardner, 1997).

TABLE 12


	Attachment	Outgrowth of	Outgrowth of TE
Treatment	(%)	ICM (%)	(%)

HSA	89.5	0.8 ± 0.1	1.8 ± 0.1
HSA + HYN	91.2	2.2 ± 0.1*	1.7 ± 0.1*
rHA + citrate	85.0	1.8 ± 0.1*	1.6 ± 0.1*
rHA + citrate + HYN	86.8	2.1 ± 0.1*	1.9 ± 0.1*

As can be seen from Table 12, development of the ICM was increased by culturing the embryos in a medium containing rHA or HYN as compared to embryos cultured in human serum albumin. [0081]

Example 11

This example illustrates that a medium containing rHA, HYN and citrate allows for the successful expansion of cryopreserved supernumerary blastocysts. [0082]
In this example, donated cryopreserved human pronucleate embryos were thawed and cultured in medium G1.3 for 48 hours followed by culturing in medium G2.3, as taught in U.S. patent application Ser. No. 09/201,594 with the following changes. The G1.2-G1.3 media has a MgSO[0083] ₄concentration from 1.0 to 1.8 and a CaCl₂concentration from 1.8 to 1.0. The changes for the G2.2-G2.3 media are the same as the changes to the G1 media, with the addition on the essential amino acids added at half the concentration and nicotinamide, inositol, and folic acid are not present.

Both media were supplemented with 2.5 mg/ml rHA and 0.125 mg/ml HYN. The freezing solution for the embryos was 4.5% glycerol and 0.1 M sucrose (10 min.) followed by 9% glycerol and 0.2 M sucrose (7 min.). The embryos were placed in a freezing machine at −6° C., seeded and held for 10 minutes, followed by cooling at 0.5° C. per minute to −32° C. The embryos were then plunged into liquid nitrogen. Immediately post thaw, the embryos were incubated individually in 500 nl of fresh G 2.3 for 4 hours after which they were placed individually in 10 microliters of G 2.3 for overnight culture. All incubations took place in 5% O ₂:6% CO₂:89% N₂The 500 nl samples of media were frozen and analyzed using ultramicrofluorescence. The glucose and pyruvate uptake of the thawed embryos was also measured.

TABLE 13


	Mean		Number of	Number of
	Glucose		Blastocysts	Blastocysts
	Uptake	Mean Pyruvate	Completely	Completely
Number of	(pmol/	Uptake	Expanded	Hatched
Blastocysts	embryo/h)	(pmol/embryo/h)	After 24 h	After 24 h

16	40.6	15.2	12 (75%)	5 (31%)

Example 12

The IVF protocol as outlined in Gardner et al. 1988 and Schoolcraft 1999 were used in this example. [0085]
This example demonstrates the advantages of a medium containing rHA, HYN and citrate on the development of human embryos. [0086]

TABLE 14

Number of Resulting Implantation

Treatment Group Patients Pregnancies Rates

HSA 10 7 (70%) 32.8%

RHA + citrate + HYN 12 9 (66.7%) 31.9%

Claims

What is claimed is:

1. A mammalian culture medium comprising recombinant human albumin and a medium that can support cell development, wherein the mammalian culture medium increases the viability of gametes or embryonic cells cultured in the mammalian culture medium, and further wherein the mammalian culture medium is free from non-recombinant human albumin.

2. The culture medium according to claim 1, wherein the medium that can support cell development is selected from the group consisting of G1.2/G2.2, KSOM/KSOMaa, M16, SOF/SOFaa, MTF, P1, HTF, Earle's, Hams F-10, M2, Hepes-G1.2, Whitten's and PBS.

3. The culture medium according to claim 1, wherein the medium that can support cell development supports embryo development.

4. The culture medium according to claim 1, wherein the medium that can support cell development supports mammalian stem cell development.

5. The culture medium according to claim 1, comprising about 0.5 mg/ml to about 5.0 mg/ml recombinant human albumin and further comprising citrate.

6. The culture medium according to claim 2, further comprising citrate.

7. The culture medium according to claim 1, comprising about 0.5 mg/ml to about 5.0 mg/ml recombinant human albumin and further comprising fermented hyaluronan.

8. The culture medium according to claim 2, further comprising fermented hyaluronan.

9. The culture medium according to claim 3, further comprising citrate.

10. The culture medium according to claim 4, further comprising citrate.

11. The culture medium according to claim 3, further comprising fermented hyaluronan.

12. The culture medium according to claim 4, further comprising fermented hyaluronan.

13. A method of increasing the viability of embryonic cells comprising culturing an embryo in the mammalian culture medium of claim 1, wherein the viability of the embryo is increased.

14. A mammalian culture medium supplement comprising recombinant human albumin, wherein the supplement increases the viability of gametes or embryonic cells cultured in a medium containing the supplement, and further wherein the supplement is free from non-recombinant human albumin.

15. The supplement according to claim 14 further comprising citrate.

16. The supplement according to claim 15, wherein the citrate is present in a range of about 0.1 mM to about 1.0 mM when added to the medium.

17. The supplement according to claim 14, wherein the recombinant human albumin is present in a range of about 0.5 mg/ml to about 5.0 mg/ml when added to the medium.

18. A method of producing a supplement for a mammalian culture medium comprising adding recombinant human albumin to either water, saline or medium to make a supplement for a mammalian culture medium, wherein the supplement increases the viability of gametes or embryonic cells cultured in a medium containing the supplement, and further wherein the supplement is free from non-recombinant human albumin.

19. The method of producing a supplement for a mammalian culture medium of claim 18 further comprising adding citrate.

20. A kit for supplementation of mammalian culture medium, comprising:

(a) a medium comprising recombinant human albumin, and optionally one or more ingredients selected from the group consisting of mammalian culture medium, fermented hyaluronan, citrate and combinations thereof, wherein the medium increases the viability of gametes or embryonic cells cultured in the medium, and further wherein the medium is free from non-recombinant human albumin; and

(b) instructions for use of the kit.