IP Library Granted Patent US 10,307,334
Granted Patent B2
US 10,307,334 · App. 15/656,634 · Granted Jun 4, 2019

Glass containers with delamination resistance and improved damage tolerance

Inventors: Theresa Chang (Painted Post, NY); Paul Stephen Danielson (Dundee, NY); Steven Edward DeMartino (Painted Post, NY); Andrei Gennadyevich Fadeev (Elmira, NY); Robert Michael Morena (Lindley, NY); Santona Pal (Painted Post, NY); John Stephen Peanasky (Big Flats, NY); Robert Anthony Schaut (Painted Post, NY); Christopher Lee Timmons (Big Flats, NY); Natesan Venkataraman (Painted Post, NY); Ronald Luce Verkleeren (Horseheads, NY)
Assignee: CORNING INCORPORATED
A61J1/1468B32B17/06B65D1/0207B65D1/0215B65D1/40B65D23/02B65D23/0814B65D23/0821B65D25/14B65D25/34B65D65/42C03C15/02C03C17/00C03C17/005C03C17/30C03C17/32C03C17/3405C03C17/42C03C21/002C09D179/08C03C2217/78C03C2218/111Y10T428/13Y10T428/131Y10T428/1317Y10T428/24802Y10T428/315
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Quick Facts
Patent No.
US 10,307,334
App. No.
15/656,634
Granted
Jun 4, 2019
Kind
B2
Abstract

In embodiments, a delamination resistant glass pharmaceutical package includes a glass body formed from a Type 1 Class glass composition according to ASTM Standard E438-92, the glass body having a wall portion with an inner surface and an outer surface. The glass body may have at least a class A2 base resistance or better according to ISO 695, at least a type HGB2 hydrolytic resistance or better according to ISO 719 and Type 1 chemical durability according to USP <660>. An interior region of the glass body may extend from about 10 nm below the inner surface and have a persistent layer homogeneity. The glass body may also have a surface region extending over the inner surface and having a persistent surface homogeneity such that the glass body is resistant to delamination.

Claims (40)

1. A delamination resistant glass pharmaceutical package comprising:

a glass body formed from a Type 1 glass composition according to ASTM Standard E438-92(2011), the glass body having a wall portion with an inner surface and an outer surface, wherein the glass body forms the inner surface of the glass pharmaceutical package, wherein the glass pharmaceutical package does not comprise a boron-rich layer on the inner surface of the glass body, and wherein the glass body is formed from a glass tube;

the glass body has at least a class A2 base resistance or better according to ISO 695, at least a type HGB2 hydrolytic resistance or better according to ISO 719 and Type 1 chemical durability according to USP <660>;

an interior region extending from about 10 nm below the inner surface and having a persistent layer homogeneity such that an extrema in a layer concentration of each constituent component of the glass composition in the interior region is greater than or equal to about 80% and less than or equal to about 120% of a concentration of the same constituent component in the glass composition at the mid-point of the thickness of the glass body when the glass body is in an as-formed condition; and

a surface region extending over the inner surface and having a persistent surface homogeneity such that the glass body is resistant to delamination such that for a discrete point on the inner surface of the glass body, an extrema of a surface concentration of each constituent component of the glass composition in the surface region at the discrete point is greater than or equal to about 70% and less than or equal to about 130% of the same constituent component in the surface region at any second discrete point on the inner surface of the glass body when the glass body is in an as-formed condition.

2. The delamination resistant glass pharmaceutical package of claim 1 , wherein the interior region has a thickness T LR of at least about 100 nm.

3. The delamination resistant glass pharmaceutical package of claim 1 , wherein a depth of the surface region is at least about 10 nm.

4. The delamination resistant glass pharmaceutical package of claim 1 , wherein a depth of the surface region is at least about 50 nm.

5. The delamination resistant glass pharmaceutical package of claim 1 , wherein the glass body was formed at a temperature greater than or equal to 1100° C. and less than or equal to about 1650° C.

6. The delamination resistant glass pharmaceutical package of claim 1 , wherein the glass body was formed under processing conditions which mitigated vaporization of species in the glass as compared with processing conditions comprising higher temperatures or faster forming speeds.

7. The delamination resistant glass pharmaceutical package of claim 1 , wherein the glass body was formed under processing conditions which imparted a uniform temperature history to the inner surface.

8. The delamination resistant glass pharmaceutical package of claim 1 , wherein the persistent layer homogeneity of the glass body is determined by dynamic secondary ion mass spectroscopy.

9. The delamination resistant glass pharmaceutical package of claim 1 , wherein the glass body was formed from a glass composition which was not phase separated.

10. The delamination resistant glass pharmaceutical package of claim 1 , wherein the glass body was formed from a glass composition that was substantially free from species which significantly volatilize at temperatures that correspond to the glass composition having a viscosity in a range from about 200 poise to about 100 kilopoise.

11. The delamination resistant glass pharmaceutical package of claim 1 , wherein the glass body is ion-exchange strengthened.

12. The delamination resistant glass pharmaceutical package of claim 1 , wherein the glass body has a delamination factor less than or equal to 10.

13. The delamination resistant glass pharmaceutical package of claim 1 , wherein

the surface region extends over the inner surface of the glass body to a depth from about 10 nm to about 50 nm from the inner surface of the glass body.

14. The delamination resistant glass pharmaceutical package of claim 13 , wherein:

the interior region extends from about 10 nm below the inner surface of the glass body into the thickness of the body and having a thickness T LR of at least about 100 nm, wherein an extrema in a layer concentration of each constituent component of glass composition in the interior region is greater than or equal to about 80% and less than or equal to about 120% of a concentration of the same constituent component in the glass composition at the mid-point of a thickness of the glass body when the glass body is in an as-formed condition.

15. The delamination resistant glass pharmaceutical package of claim 1 , wherein

the interior region extends from about 10 nm below the inner surface of the glass body into the thickness of the glass body and having a thickness T LR of at least about 100 nm.

16. The delamination resistant glass pharmaceutical package of claim 1 , wherein the glass pharmaceutical package comprises one or both of a compressive stress layer or a lubricous coating.

17. A delamination resistant glass pharmaceutical package comprising:

a glass body formed from an ion-exchangeable Type 1 glass composition according to ASTM Standard E438-92(2011), the glass body having a wall portion with an inner surface, an outer surface, and having a thickness with a mid-point therebetween, wherein the glass body forms the inner surface of the glass pharmaceutical package, wherein the glass pharmaceutical package does not comprise a boron-rich layer on the inner surface of the glass body, and wherein the glass body is formed from a glass tube;

the glass body has at least a class A2 base resistance or better according to ISO 695, at least a type HGB2 hydrolytic resistance or better according to ISO 719 and Type 1 chemical durability according to USP <660>;

an interior region extending from about 10 nm below the inner surface of the glass body into a thickness of the glass body and having a thickness T LR of at least about 100 nm, wherein an extrema in a layer concentration of each constituent component of the glass composition in the interior region is within ±20% of a concentration of the same constituent component in the glass composition at the mid-point of the thickness the glass body when the glass body is in an as-formed condition; and

a surface region extending over the entire inner surface of the glass body to a depth of about 10 nm from the inner surface of the glass body, wherein, for a discrete point on the inner surface of the glass body, an extrema of a surface concentration of each constituent component in the surface region at the discrete point is within ±30% of a concentration of the same constituent component in the surface region at any second discrete point on the inner surface of the glass body when the glass body is in an as-formed condition.

18. The delamination resistant glass pharmaceutical package of claim 17 , wherein the extrema in the layer concentration of each constituent component in the interior region is greater than or equal to about 90% and less than or equal to about 110% of a concentration of the same constituent component at the mid-point.

19. The delamination resistant glass pharmaceutical package of claim 17 , wherein the extrema of the surface concentration of each constituent component of the glass composition in the surface region at the discrete point is greater than or equal to about 85% and less than or equal to about 115% of the same constituent component in the surface region at any second discrete point on the inner surface when the glass body is in an as-formed condition.

20. The delamination resistant glass pharmaceutical package of claim 17 , wherein the glass body has a delamination factor less than or equal to 10.

21. The delamination resistant glass pharmaceutical package of claim 17 , wherein the glass body was formed under processing conditions which mitigated vaporization of species in the glass as compared with processing conditions comprising higher temperatures or faster forming speeds.

22. The delamination resistant glass pharmaceutical package of claim 17 , wherein the glass body was formed under processing conditions which imparted a uniform temperature history to the inner surface.

23. The delamination resistant glass pharmaceutical package of claim 17 , wherein the glass body was formed from a glass composition which was not phased separated.

24. The delamination resistant glass pharmaceutical package of claim 17 , wherein the glass pharmaceutical package comprises one or both of a compressive stress layer or a lubricous coating.

25. A delamination resistant glass pharmaceutical package comprising:

a glass body formed from a Type 1 glass composition according to ASTM Standard E438-92(2011), the glass body having a wall portion with an inner surface, an outer surface, and having a thickness with a mid-point therebetween and comprising a wall portion that transitions to a floor portion through a heel portion, wherein the glass body forms the inner surface of the glass pharmaceutical package, wherein the glass pharmaceutical package does not comprise a boron-rich layer on the inner surface of the glass body, and wherein the glass body is formed from a glass tube;

the glass body has at least a class A2 base resistance or better according to ISO 695, at least a type HGB2 hydrolytic resistance or better according to ISO 719 and Type 1 chemical durability according to USP <660>; and

a surface region extending over at least the inner surface and having a depth extending from the inner surface of the glass container into the thickness of the glass body, the surface region having a persistent surface homogeneity such that that for a discrete point on the inner surface of the glass body, an extrema of a surface concentration of each constituent component of the glass composition in the surface region at the discrete point is greater than or equal to about 70% and less than or equal to about 130% of the same constituent component in the surface region at any second discrete point on the inner surface of the glass body when the glass body is in an as-formed condition.

26. The delamination resistant glass pharmaceutical package of claim 25 , wherein the glass pharmaceutical package comprises one or both of a compressive stress layer or a lubricous coating.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 27, 2018
From: CHANG, THERESA; DANIELSON, PAUL STEPHEN; DEMARTINO, STEVEN EDWARD; FADEEV, ANDREI GENNADYEVICH; MORENA, ROBERT MICHAEL; PAL, SANTONA; PEANASKY, JOHN STEPHEN; SCHAUT, ROBERT ANTHONY; VENKATARAMAN, NATESAN; VERKLEEREN, RONALD LUCE; TIMMONS, CHRISTOPHER LEE
To: CORNING INCORPORATED
Reel/Frame 046716/0806 →
Continuity (3)
Continuation 14075620 · Nov 8, 2013
Provisional Application 61731767 · Nov 30, 2012
Related Publication 20170320773A1 · Nov 9, 2017
Cited By (1)
US 12,344,544